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Article

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

Neuropathology : official journal of the Japanese Society of Neuropathology - 1 Oct 2023

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

Abstract excerpt

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 that were discovered incidentally. No apparent spatial connection was observed on preoperative magnetic resonance...

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Identifiers

PMID: 36942363
DOI: 10.1111/neup.12902

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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