Rare clinical form of glioblastoma multiforme

COMMENTARY ON THE LAW

Rare clinical form of glioblastoma multiforme

Maria Ejma 1 , Marta Waliszewska-Prosół 1 , Anna Hofman 1 , Joanna Bladowska 2 , Lesław Wojciech Zub 3

1. Klinika Neurologii, Uniwersytet Medyczny we Wrocławiu
2. Zakład Radiologii Ogólnej, Zabiegowej i Neuroradiologii, Uniwersytet Medyczny we Wrocławiu
3. Klinika Neurochirurgii, Uniwersytet Medyczny we Wrocławiu

Published: 2014-03-27
DOI: 10.5604/17322693.1095834
GICID: 01.3001.0003.1207
Available language versions: en pl
Issue: Postepy Hig Med Dosw 2014; 68 : 316-324

 

Abstract

Glioblastoma multiforme (glioblastoma multiforme – GBM) is the most malignant tumor classified by WHO. It is also the most common primary CNS tumor with a very aggressive course and unfavourable prognosis, usually develops in adults, and is typically located supratentorially in the fronto-temporal region. However, the literature describes an unusual position of GBM (e.g. spinal cord, pons, pineal region), familial gliomas unconnected with the family of gliomas predisposed to the occurrence of syndromes, unusual glioma and metastatic sites, gliomas transplanted with organs. In this paper, based on the available literature, the authors discuss an unusual and rare form of glioblastoma multiforme.

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