Ismail S M, Cole G
J Neurosurg. 1984 Jun;60(6):1279-81. doi: 10.3171/jns.1984.60.6.1279.
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.
作者描述了一例在尸检时被诊断为冯·希佩尔-林道综合征的49岁女性病例。她因小脑成血管细胞瘤出血而突然死亡。其他尸检发现包括视网膜成血管细胞瘤、肾上腺嗜铬细胞瘤和肾透明细胞肿瘤。该病例的独特之处在于意外发现了多个脊神经根微小成血管细胞瘤。本文对该病例进行了讨论,重点是冯·希佩尔-林道综合征中脊髓成血管细胞瘤的发病率。