85583005: Pheochromocytoma (morphologic abnormality)

SNOMED CT Concept\Body structure (body structure)\Morphologically altered structure\Morphologically abnormal structure\...

\Growth alteration\Proliferation\Proliferative mass (morphologic abnormality)\Neoplasm and/or hamartoma (morphologic abnormality)\Neoplasm\Neuroendocrine neoplasm\Paraganglioma AND/OR glomus tumor\Pheochromocytoma

\Lesion (morphologic abnormality)\Mass\Proliferative mass (morphologic abnormality)\Neoplasm and/or hamartoma (morphologic abnormality)\Neoplasm\Neuroendocrine neoplasm\Paraganglioma AND/OR glomus tumor\Pheochromocytoma

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

141864017 Pheochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

141866015 Chromaffin paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

141867012 Chromaffin tumor en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

141868019 Chromaffinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

141870011 Phaeochromocytoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

201225012 Adrenal medullary paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

506611012 Chromaffin tumour en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

827667018 Pheochromocytoma (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3782047015 Chromaffin cell neoplasm 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
Pheochromocytoma	Is a	Neoplasm	false	Inferred relationship	Some
Pheochromocytoma	Is a	Chromaffin cell neoplasm	false	Inferred relationship	Some
Pheochromocytoma	Is a	Paraganglioma AND/OR glomus tumor	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Benign pheochromocytoma (morphologic abnormality)	Is a	True	Pheochromocytoma	Inferred relationship	Some
Catecholamine secretion by pheochromocytoma	Associated morphology	False	Pheochromocytoma	Inferred relationship	Some	1
Phaeochromocytoma	Associated morphology	True	Pheochromocytoma	Inferred relationship	Some	1
Catecholamine secretion by pheochromocytoma	Associated morphology	True	Pheochromocytoma	Inferred relationship	Some	1
A rare, hereditary, pheochromocytoma/paraganglioma tumor arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from any paraganglia from the skull base to the pelvic floor (paraganglioma). Clinical manifestations are often linked to excess catecholamines production causing sustained or paroxysmal elevations in blood pressure, headache, episodic profuse sweating, palpitations, pallor and apprehension or anxiety. Hereditary pheochromocytoma/paraganglioma tumors tend to present at younger ages, to be multi-focal, bilateral, and recurrent, or to have multiple synchronous neoplasms.	Associated morphology	True	Pheochromocytoma	Inferred relationship	Some	2
A potentially lethal complication of pheochromocytoma that may occur as a result of anaesthesia, surgery or during pregnancy and childbirth. The crisis is caused by excessive release of catecholamines and may be drug-induced secondary to histamine release, dopamine receptor blockade, or sympathomimetic action. Crisis may also result from mechanical factors such as squeeze of the tumour during surgery.	Associated morphology	True	Pheochromocytoma	Inferred relationship	Some	1
A rare, isolated, non-familial pheochromocytoma/paraganglioma tumor arising from neuroendocrine chromaffin cells of the adrenal medulla (pheochromocytoma) or from extra-adrenal chromaffin tissue (paraganglioma). The majority of these tumors are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumor, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.	Associated morphology	True	Pheochromocytoma	Inferred relationship	Some	2
Malignant phaeochromocytoma	Is a	True	Pheochromocytoma	Inferred relationship	Some
Composite pheochromocytoma (morphologic abnormality)	Is a	True	Pheochromocytoma	Inferred relationship	Some

This concept is not in any reference sets