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.
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Acknowledgments
We thank the CJ Foundation for SIDS and First Candle/SIDS Alliance for providing grant support for this study. We also thank the San Diego Guild for Infant Survival, the Guild for Infant Survival of Orange County, and the many families and friends of children who have died suddenly and unexpectedly and have contributed so generously to the San Diego SIDS/SUDC Research Project.
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Wixom, C., Chadwick, A.E. & Krous, H.F. Sudden, Unexpected Death Associated with Meningioangiomatosis: Case Report. Pediatr Dev Pathol 8, 240–244 (2005). https://doi.org/10.1007/s10024-004-9105-4
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DOI: https://doi.org/10.1007/s10024-004-9105-4