Ganglioglioma pathophysiology: Difference between revisions

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==Pathophysiology==
==Pathophysiology==
===Gross Pathology===
===Gross Pathology===
There is predilection towards the [[temporal lobes]].
There is predilection towards the [[temporal lobes]].


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It is the grade of the glial component that determines biological behaviour. Dedifferentiation into high grade tumours does occasionally occur, and it is usually the glial component (into a [[glioblastoma multiforme]]). Only rarely is it the neuronal component (into a [[neuroblastoma]]).
It is the grade of the glial component that determines biological behaviour. Dedifferentiation into high grade tumours does occasionally occur, and it is usually the glial component (into a [[glioblastoma multiforme]]). Only rarely is it the neuronal component (into a [[neuroblastoma]]).
===Markers===
Neuronal origin is demonstrated by positivity to neuronal markers:
*Synaptophysin
*Neuronal specific enolase
*''GFAP'' marker


==References==
==References==

Revision as of 14:19, 3 September 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]

Overview

Pathophysiology

Gross Pathology

There is predilection towards the temporal lobes.

Microscopic Pathology

Gangliogliomas are composed of two cell populations:

  • Ganglion cells (large mature neuronal elements): ganglio-
  • Neoplastic glial elements (primarily astrocytic): -glioma

It is the grade of the glial component that determines biological behaviour. Dedifferentiation into high grade tumours does occasionally occur, and it is usually the glial component (into a glioblastoma multiforme). Only rarely is it the neuronal component (into a neuroblastoma).

Markers

Neuronal origin is demonstrated by positivity to neuronal markers:

  • Synaptophysin
  • Neuronal specific enolase
  • GFAP marker

References


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