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

Ikeda, H; Yamaguchi, S; Ishi, Y; Wakabayashi, K; Shimizu, A; Kanno-Okada, H; Endo, T; Ota, M; Okamoto, M; Motegi, H; Iwasaki, N; Fujimura, M

Ishi, Y (通讯作者)，Hokkaido Univ, Dept Neurosurg, Grad Sch Med, North 15 West7, Kita Ku, Sapporo 0608638, Japan.

NEUROPATHOLOGY, 2023; 43 (5): 413

Abstract

Somatic mosaicism of isocitrate dehydrogenase 1/2 (IDH1/2) mutation is a cause of Ollier disease (OD), characterized by multiple enchondromatosis. A 3......

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