Paraganglioma: Difference between revisions

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==[[Paraganglioma overview|Overview]]==
==[[Paraganglioma overview|Overview]]==


==Inheritance==
==[[Paraganglioma causes|Causes of Paraganglioma]]==
Familial paragangliomas account for approx. 25% of cases, are often multiple and bilateral, and occur at an earlier age.  Mutations of the genes [[SDHD]] (previously known as PGL1), [[PGL2]], and [[SDHC (gene)|SDHC]] (previously PGL3) have been identified as causing familial head and neck paragangliomas. Mutations of [[SDHB]] play an important role in familial adrenal pheochromocytoma and extra-adrenal paraganglioma (of abdomen and thorax), although there is considerable overlap in the types of tumors associated with SDHB and SDHD gene mutations.


==[[Paraganglioma pathophysiology|Pathophysiology]]==
==[[Paraganglioma pathophysiology|Pathophysiology]]==

Revision as of 19:04, 20 January 2012

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Paraganglioma
ICD-O: 8680-8700
DiseasesDB 33480

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

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The main treatment modalities are surgery, embolization and radiotherapy.

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