| Literature DB >> 29682141 |
Ryo Miyahara1, Satoshi Tsutsumi1, Satoshi Adachi2, Hisato Ishii1, Akihide Kondo2, Yukimasa Yasumoto1.
Abstract
A 26-year-old woman with familial neurofibromatosis type 1 sustained headache that worsened for 1 month. Neuroimaging revealed a mild ventriculomegaly and nonenhancing lesion in the pons. In spite of repeated cerebrospinal fluid examinations and magnetic resonance imaging, the etiology was not determined. The affected pons markedly enlarged in the following 2 months, with extensive leptomeningeal dissemination. Biopsy through hemilaminectomy of the T9 was diagnosed as glioblastoma multiforme. Prompt histologic examination should be performed when patients with familial neurofibromatosis type 1 manifest communicating hydrocephalus coexistent with a nonenhancing tumor.Entities:
Keywords: Communicating hydrocephalus; Leptomeningeal GBM; Neurofibromatosis type 1; Nonenhancing pontine tumor
Year: 2018 PMID: 29682141 PMCID: PMC5909025 DOI: 10.1016/j.radcr.2018.03.021
Source DB: PubMed Journal: Radiol Case Rep ISSN: 1930-0433