Glioblastoma multiforme pathophysiology: Difference between revisions

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* Almost all cases of GBM are sporadic, without a familial predilection, although [[chromosome|chromosomal]] aberrations such as [[PTEN (gene)|PTEN]] mutation, and [[p53]] mutation are commonly seen in these tumors.
* Almost all cases of GBM are sporadic, without a familial predilection, although [[chromosome|chromosomal]] aberrations such as [[PTEN (gene)|PTEN]] mutation, and [[p53]] mutation are commonly seen in these tumors.
* Growth factor aberrant signaling associated with [[Epidermal_growth_factor_receptor|EGFR]], and [[PDGF]] are also seen.
* Growth factor aberrant signaling associated with [[Epidermal_growth_factor_receptor|EGFR]], and [[PDGF]] are also seen.
===Associated Conditions===
Glioblastoma may be associated with:<ref name=ddd>Pathology of glioblastoma multiforme. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/glioblastoma</ref>
*Neurofibromatosis type 1
*[[Li-Fraumeni syndrome]]
*[[Turcot syndrome]]
*[[Ollier disease]]
*[[Maffucci syndrome]]


===Gross Pathology===
===Gross Pathology===

Revision as of 17:49, 12 September 2015

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

Overview

Pathophysiology

Genetics

  • Almost all cases of GBM are sporadic, without a familial predilection, although chromosomal aberrations such as PTEN mutation, and p53 mutation are commonly seen in these tumors.
  • Growth factor aberrant signaling associated with EGFR, and PDGF are also seen.

Associated Conditions

Glioblastoma may be associated with:[1]

Gross Pathology

Microscopic Pathology

References

  1. Pathology of glioblastoma multiforme. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/glioblastoma


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