Literature DB >> 24054724

A case of oligodendroglioma with prominent neuronal differentiation.

Takanori Hirose1, Sumihito Nobusawa, Yoichi Nakazato, Atsushi Sasaki.   

Abstract

We report a case of oligodendroglioma showing marked neuronal differentiation, which arose in the right frontal lobe of a 46-year-old woman. The resected tumor was composed of a mixture of oligodendroglioma, gangliocytoma, and neurocytoma areas with predominance of gangliocytoma-like areas. The oligodendroglioma areas showed immunoreactivity for Olig2 and mutant isocitrate dehydrogenase 1 protein, whereas the gangliocytoma and neurocytoma areas were positive for synaptophysin and NeuN. Ki-67 labeling index was approximately 5% to 10% in the oligodendroglioma areas. Molecular cytogenetic analyses demonstrated chromosomal losses of 1p and 19q and a mutation of isocitrate dehydrogenase 1 (G395A, R132H) in both the oligodendroglioma and gangliocytoma areas. These data suggest that this tumor is an oligodendroglioma associated with prominent neuronal differentiation. There seems to be a close relationship between oligodendroglial progenitor cells and neuronal cells.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Keywords:  Gangliocytoma; IDH1; Neurocytoma; Neuronal differentiation; Oligodendroglioma

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Year:  2013        PMID: 24054724     DOI: 10.1016/j.humpath.2013.02.013

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  1 in total

1.  IDH-mutated astrocytomas with 19q-loss constitute a subgroup that confers better prognosis.

Authors:  Ryohei Otani; Takeo Uzuka; Fumi Higuchi; Hadzki Matsuda; Masashi Nomura; Shota Tanaka; Akitake Mukasa; Koichi Ichimura; Phyo Kim; Keisuke Ueki
Journal:  Cancer Sci       Date:  2018-06-15       Impact factor: 6.716

  1 in total

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