302833002: Paraganglioma (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\...

\Neuroendocrine neoplasm (disorder)\Paraganglioma

\Neoplastic disease of uncertain behavior\Paraganglioma

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

444769017 Paraganglioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

698992010 Paraganglioma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

960501000195117 paraganglioma it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

823451000241110 paragangliome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Paraganglioma	Is a	Neoplasm of paraganglion	false	Inferred relationship	Some
Paraganglioma	Associated morphology	Neoplasm	false	Inferred relationship	Some	3
Paraganglioma	Finding site	Paraganglia structure	false	Inferred relationship	Some	3
Paraganglioma	Pathological process	Neoplastic process	false	Inferred relationship	Some
Paraganglioma	Finding site	Anatomical structure	false	Inferred relationship	Some	3
Paraganglioma	Is a	Neoplastic disease of uncertain behavior	true	Inferred relationship	Some
Paraganglioma	Is a	tumeur neuroendocrine	false	Inferred relationship	Some
Paraganglioma	Associated morphology	Paraganglioma	true	Inferred relationship	Some	1
Paraganglioma	Is a	Neuroendocrine neoplasm (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Gangliocytic paraganglioma	Is a	True	Paraganglioma	Inferred relationship	Some
Extra-adrenal paraganglioma	Is a	False	Paraganglioma	Inferred relationship	Some
Neoplasm of para-aortic body	Is a	False	Paraganglioma	Inferred relationship	Some
Chromaffinoma	Is a	False	Paraganglioma	Inferred relationship	Some
Chromaffin paraganglioma	Is a	False	Paraganglioma	Inferred relationship	Some
Benign neoplasm of carotid body	Is a	False	Paraganglioma	Inferred relationship	Some
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.	Is a	True	Paraganglioma	Inferred relationship	Some
Carney-Stratakis syndrome is a recently described familial syndrome characterized by gastrointestinal stromal tumors (GIST) and paragangliomas, often at multiple sites.	Is a	True	Paraganglioma	Inferred relationship	Some
A rare neuroendocrine tumor arising from neural crest-derived paraganglion cells (most often in the para-aortic region at the level of renal hilum, organ of Zuckerkandl, thoracic paraspinal region, bladder, and carotid body) not associated with catecholamine secretion. These tumors are usually clinically silent and symptoms, if present, are nonspecific and depend on the location of the tumor. Association with certain hereditary cancer-predisposing syndromes, such as multiple endocrine neoplasia, neurofibromatosis type 1 or von Hippel Lindau syndrome, may be observed.	Is a	True	Paraganglioma	Inferred relationship	Some
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.	Is a	True	Paraganglioma	Inferred relationship	Some
A rare, endocrine disease characterized by early onset of polycythemia, and later occurring multiple paraganglioma. Clinical presentation includes hypertension, headaches, fatigue, nausea, anxiety, and high concentration of red blood cells, leading to increased risk of stroke and pulmonary thromboembolism.	Is a	True	Paraganglioma	Inferred relationship	Some

This concept is not in any reference sets