Anaplastic oligodendroglioma arising from the brain stem and featuring 1p/19q co-deletion.

Détails

ID Serval
serval:BIB_A51580D78AE5
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Anaplastic oligodendroglioma arising from the brain stem and featuring 1p/19q co-deletion.
Périodique
Neuropathology
Auteur⸱e⸱s
Hewer E., Beck J., Vassella E., Vajtai I.
ISSN
1440-1789 (Electronic)
ISSN-L
0919-6544
Statut éditorial
Publié
Date de publication
02/2014
Peer-reviewed
Oui
Volume
34
Numéro
1
Pages
32-38
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article
Publication Status: ppublish
Résumé
With respect to localization, oligodendrogliomas are characterized by a marked preponderance of the cerebral hemispheres. Outside these typical sites, any tumor histopathologically reminiscent of oligodendroglioma a priori is likely to represent one of its morphological mimics, including clear cell ependymoma, neurocytoma, pilocytic astrocytoma or glioneuronal tumors. This is particularly relevant as several of the latter are in principle curable by surgery. Among extrahemispherical sites, bona fide oligodendroglioma - as characterized by loss of heterozygosity (LOH) of chromosome arms 1p and 19q - so far has not been documented to occur in the brain stem. Here, we report the case of a 55-year-old female patient with an anaplastic oligodendroglioma (WHO grade III) of the brain stem and cerebellum diagnosed by stereotactic biopsy and featuring combined LOH of 1p and 19q. A morphological peculiarity was a population of interspersed tumor giant cells, a phenomenon that has been referred to as polymorphous oligodendroglioma. Our findings confirm the notion that - although very infrequently - true oligodendrogliomas do occur in the infratentorial compartment.
Mots-clé
Brain Stem Neoplasms/diagnosis, Brain Stem Neoplasms/genetics, Brain Stem Neoplasms/pathology, Chromosome Deletion, Chromosomes, Human, Pair 1/genetics, Chromosomes, Human, Pair 19/genetics, Female, Humans, Middle Aged, Oligodendroglioma/diagnosis, Oligodendroglioma/genetics, Oligodendroglioma/pathology, brain stem, cerebellum, differential diagnosis, loss of heterozygosity, oligodendroglioma
Pubmed
Web of science
Création de la notice
31/08/2020 13:02
Dernière modification de la notice
10/11/2020 7:26
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