Saranga R, Matzkin H, Papo J, Braf Z
Department of Urology, Tel-Aviv Medical Center, Ichilov Hospital, Israel.
Urology. 1989 Nov;34(5):301-4. doi: 10.1016/0090-4295(89)90330-0.
Two cases are reported of von Hippel-Lindau syndrome in two brothers. One had an asymptomatic adrenal pheochromocytoma (probably bilateral) and a synchronous metastatic hypernephroma which presented as a rather "innocent" renal colic. The second asymptomatic brother underwent urologic investigation which revealed multifocal tumors of the kidney. High clinical suspicion based on family history only is mandatory. The literature related to von Hippel-Lindau syndrome is reviewed.
报告了两兄弟患冯·希佩尔-林道综合征的病例。其中一人患有无症状肾上腺嗜铬细胞瘤(可能为双侧)和同步转移性肾细胞癌,表现为相当“隐匿”的肾绞痛。第二名无症状的兄弟接受了泌尿科检查,发现有肾脏多灶性肿瘤。仅基于家族史进行高度临床怀疑是必要的。对与冯·希佩尔-林道综合征相关的文献进行了综述。