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Article

Solitary epicranial neurofibroma with NF1-related germline mutation: case report.

Neurologia medico-chirurgica - 1 Jan 2014

Sugiyama Natsuki, Tsutsumi Satoshi, Akiba Chihiro, Nakanishi Hajime, Ogino Ikuko, Yasumoto Yukimasa, Arai Hajime, Ito Masanori

Abstract excerpt

A 33-year-old male became aware of a painless soft mass in the left occipital region. His medical and family history were unremarkable for neurofibromatosis type 1 (NF1) or other genetic disorders. Physical examination showed no signs of NF1. Neurological and ophthalmological examinations found no abnormality. Cranial computed tomography showed an isodense mass located subcutaneously with irregular deformities in...

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Identifiers

PMID: 24140765
DOI: 10.2176/nmc.cr2012-0364
PMCID: PMC4533480

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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