Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report

Somatic mosaicism of isocitrate dehydrogenase 1/2 (IDH1/2) mutation is a cause of Ollier disease (OD), characterized by multiple enchondromatosis. A 35-year-old woman who was diagnosed with OD at age 24 underwent resection surgery for multifocal tumors located at the right and left frontal lobes tha...

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Veröffentlicht in:	Neuropathology 2023-10, Vol.43 (5), p.413-420
Hauptverfasser:	Ikeda, Hiroshi, Yamaguchi, Shigeru, Ishi, Yukitomo, Wakabayashi, Kento, Shimizu, Ai, Kanno-Okada, Hiromi, Endo, Takeshi, Ota, Mitsutoshi, Okamoto, Michinari, Motegi, Hiroaki, Iwasaki, Norimasa, Fujimura, Miki
Format:	Artikel
Sprache:	eng
Schlagworte:	Astrocytoma Brain cancer Brain tumors Case reports DNA sequencing Fluorescence in situ hybridization Frontal lobe Glioma Isocitrate dehydrogenase Magnetic resonance imaging Mosaicism Mutants Mutation Oligodendroglioma Peripheral blood Tumor cells Tumors
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