| Literature DB >> 6539366 |
Abstract
The authors describe a case of von Hippel-Lindau syndrome diagnosed at autopsy in a 49-year-old woman. She died suddenly following hemorrhage from a cerebellar hemangioblastoma. Other autopsy findings included a retinal hemangioblastoma, an adrenal pheochromocytoma, and a clear-cell renal tumor. The case was distinguished by the unexpected finding of multiple microscopic hemangioblastomas of the spinal nerve roots. The case is discussed with emphasis on the incidence of spinal hemangioblastomas in von Hippel-Lindau syndrome.Entities:
Mesh:
Year: 1984 PMID: 6539366 DOI: 10.3171/jns.1984.60.6.1279
Source DB: PubMed Journal: J Neurosurg ISSN: 0022-3085 Impact factor: 5.115