| Literature DB >> 31257192 |
Akari Kimura1, Yoichiro Takahashi1, Kunio Mizutari1, Hironori Tsujimoto2, Kuniaki Nakanishi3, Akihiro Shiotani1.
Abstract
We describe a rare case of meningeal carcinomatosis (MC) in a 66-year-old man who presented with bilateral deafness and vertigo, initially presumed to be neurofibromatosis type-2. Brain magnetic resonance imaging (MRI) of the patient revealed bilateral gadolinium enhanced masses at the cerebellopontine angle. However, multiple central nervous system symptoms, including loss of consciousness, gradually appeared. He had a history of gastric cancer; therefore, a lumbar puncture was performed. Cytological examination of the cerebrospinal fluid confirmed the presence of adenocarcinoma cells. The general condition of this patient worsened, and he died 46 days after the first onset of hearing loss. An autopsy was performed, and multiple infiltrations of adenocarcinoma cells in the brain were confirmed, though undetected by MRI. The prognosis of MC is extremely poor; therefore, rapid diagnosis is important to prevent mortality. Retrospectively, a lumbar puncture could have been conducted earlier to identify MC, especially in consideration of the clinical history of this patient.Entities:
Year: 2019 PMID: 31257192 PMCID: PMC6750794 DOI: 10.5152/iao.2019.6080
Source DB: PubMed Journal: J Int Adv Otol ISSN: 1308-7649 Impact factor: 1.017