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
Ganglioglioma Microchapters |
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Risk calculators and risk factors for Ganglioglioma pathophysiology |
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