• Kate E Ahmad, Suad Al-Jahdhami, and Omar Ahmad.
• Department of Neurology, The Canberra Hospital, Australian Capital Territory 2611, Australia.
• J Clin Neurosci. 2010 Dec 1; 17 (12): 1581-2.

AbstractRhabdoid meningiomas are rare, aggressive tumours of the meninges that have a generally poor prognosis. We report a 49-year-old man with a background history of sarcoidosis who presented with nausea and vomiting. Imaging showed generalised leptomeningeal and subependymal enhancement suggestive of chronic meningitis. He had multiple lumbar punctures and a brain biopsy, none of which led to a pathological diagnosis. He died within months, and a postmortem examination was performed. At this stage, a diagnosis of rhabdoid meningioma was made. The clinical and radiological presentation of rhabdoid meningioma as a diffuse leptomeningeal process without a mass lesion is unique. All other published cases of rhabdoid meningioma have been of a discrete lesion. This highlights the importance of a tissue diagnosis in patients where the imaging is non-specific. A brief review of rhabdoid meningioma follows.Crown Copyright © 2010. Published by Elsevier Ltd. All rights reserved.

18 keywords...

hide…