| Literature DB >> 15803213 |
Chris Wixom1, Amy E Chadwick, Henry F Krous.
Abstract
We report a case of sudden, unexpected death associated with meningioangiomatosis in a 13-year-old, previously healthy male without a history of seizures, neurologic deficits, or clinical stigmata of neurofibromatosis. There was no family history of neurofibromatosis. The postmortem examination showed a 5-cm mass involving the right posterior frontal and orbital frontal cortex that had microscopic features diagnostic of meningioangiomatosis. Because no other cause of death was found, we postulate that he likely died as a result of a seizure secondary to meningioangiomatosis.Entities:
Mesh:
Year: 2005 PMID: 15803213 DOI: 10.1007/s10024-004-9105-4
Source DB: PubMed Journal: Pediatr Dev Pathol ISSN: 1093-5266