Vanacker P, Vanacker A, Leys A, Thijs V
Department of Neurology, University Hospitals Leuven, Leuven, Belgium.
Acta Clin Belg. 2010 Jul-Aug;65(4):279-80. doi: 10.1179/acb.2010.060.
We report on a 34-year-old woman, who was recently diagnosed with Von Hippel-Lindau disease (VHL), genetically confirmed. At this moment, she presented with an acute history of arterial hypertension, headache, cortical blindness and epilepsy. On the basis of clinical and magnetic resonance imaging (MRI) criteria the diagnosis of a posterior reversible encephalopathy syndrome (PRES) was made. A iodine 123-Labeled metaiodobenzylguanidine (MIBG) scan revealed the presence of bilateral adrenal pheochromocytomas.
我们报告了一名34岁女性，她最近被基因确诊为冯·希佩尔-林道病（VHL）。目前，她出现了动脉高血压、头痛、皮质盲和癫痫的急性病史。根据临床和磁共振成像（MRI）标准，诊断为后部可逆性脑病综合征（PRES）。碘123标记的间碘苄胍（MIBG）扫描显示双侧肾上腺嗜铬细胞瘤的存在。
