| Literature DB >> 24054724 |
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.Entities:
Keywords: Gangliocytoma; IDH1; Neurocytoma; Neuronal differentiation; Oligodendroglioma
Mesh:
Substances:
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