1268352008: Primary carcinoma of pituitary gland (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Neoplasm of head\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Neoplasm of head\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.

\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant epithelial neoplasm of endocrine gland (disorder)\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Neoplasm of head\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Mass of head (finding)\Intracranial mass\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Mass of body region\Mass of head and/or neck (finding)\Neoplasm of head and neck\Neoplasm of head\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Primary malignant neoplasm of nervous system\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.

\Neurological lesion\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Primary malignant neoplasm of nervous system\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.

\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Pituitary mass\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Mass lesion of brain (finding)\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.

\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant epithelial neoplasm of endocrine gland (disorder)\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant epithelial neoplasm (disorder)\Primary malignant epithelial neoplasm of endocrine gland (disorder)\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant epithelial neoplasm (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Primary malignant neoplasm (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant epithelial neoplasm of endocrine gland (disorder)\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Primary malignant neoplasm (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Primary malignant neoplasm (disorder)\Primary malignant neoplasm of nervous system\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Primary malignant neoplasm (disorder)\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of nervous system (disorder)\Primary malignant neoplasm of nervous system\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant epithelial neoplasm of endocrine gland (disorder)\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of head and/or neck (disorder)\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Malignant neoplasm of head and/or neck (disorder)\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of head and neck\Neoplasm of head\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Primary malignant neoplasm of nervous system\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant epithelial neoplasm of endocrine gland (disorder)\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of endocrine gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Malignant neoplasm of endocrine gland (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of endocrine system\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Malignant neoplasm of nervous system (disorder)\Primary malignant neoplasm of nervous system\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Neoplasm of nervous system\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Malignant neoplasm of central nervous system (disorder)\Primary malignant neoplasm of central nervous system\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Neoplasm of central nervous system\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Intracranial neoplasm\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Neoplasm of head\Primary malignant neoplasm of head\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant epithelial neoplasm of brain (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Malignant neoplasm of brain (disorder)\Primary malignant neoplasm of brain\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Malignant neoplasm of cerebrum (disorder)\Primary malignant neoplasm of cerebrum\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Pituitary carcinoma\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Lesion of brain\Neoplasm of brain\Neoplasm of cerebrum\Neoplasm of pituitary gland\Malignant neoplasm of pituitary gland (disorder)\Primary malignant neoplasm of pituitary gland\A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5400486013 A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5400487016 A rare pituitary tumour characterised by the presence of a pituitary adenoma that has metastasised either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumours behave aggressively, and prognosis is poor. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5179265014 Primary pituitary carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5179266010 Primary carcinoma of pituitary gland (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5179268011 Primary carcinoma of pituitary gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	Is a	Pituitary carcinoma	true	Inferred relationship	Some
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	Is a	Primary malignant epithelial neoplasm of endocrine gland (disorder)	true	Inferred relationship	Some
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	Is a	Primary malignant neoplasm of pituitary gland	true	Inferred relationship	Some
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	Finding site	Pituitary structure	true	Inferred relationship	Some	1
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	Associated morphology	Carcinoma (morphologic abnormality)	true	Inferred relationship	Some	1
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	Pathological process (attribute)	Malignant proliferation of primary neoplasm (qualifier value)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
5400486013	A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400487016	A rare pituitary tumour characterised by the presence of a pituitary adenoma that has metastasised either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumours behave aggressively, and prognosis is poor.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5179265014	Primary pituitary carcinoma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5179266010	Primary carcinoma of pituitary gland (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5179268011	Primary carcinoma of pituitary gland	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core