Gundlach P, Stern J
Neurochirurgia (Stuttg). 1982 Jul;25(4):124-8. doi: 10.1055/s-2008-1053975.
A case of incomplete von Hippel-Lindau's disease is described. Our patient is characterized by multilocular and recurring typical hemangioblastomas in the cerebellum and the spinal cord. Moreover there are hints at familiar pre-disposition. Based on the recent literature the morphological and clinical characteristics are discussed with special consideration of modern radiological (myelography, arteriography, computertomography) and laboratory (hemoglobin levels follow-ups) investigations.
本文描述了一例不完全性冯·希佩尔-林道病。我们的患者表现为小脑和脊髓内多发、复发性典型血管母细胞瘤。此外,有家族易患倾向的迹象。基于近期文献,结合现代放射学(脊髓造影、动脉造影、计算机断层扫描)和实验室(血红蛋白水平随访)检查,对其形态学和临床特征进行了讨论。