Ertas Gulcin, Altundag Muzaffer Bedri, Ucer Ali Riza, Cankal Fatih, Altundag Kadri
Department of Radiation Oncology, Ankara Oncology Hospital, Ankara, Turkey.
J Neurooncol. 2005 Jul;73(3):273-5. doi: 10.1007/s11060-004-5179-0.
Von Hippel-Lindau Disease, a multisystem familial cancer syndrome, is inherited as an autosomal-dominant trait. Common manifestations of the disease are retinal, cerebellar and medullary hemangioblastomas; renal cysts and carcinomas; pancreatic cysts; pheochromocytoma; and papilllary cystadenoma of the epididym. We report the case of a 40-year-old man with type I von Hippel-Lindau disease treated with external radiotherapy for recurrent cerebellar hemangioblastoma.
冯·希佩尔-林道病是一种多系统家族性癌症综合征，以常染色体显性特征遗传。该疾病的常见表现包括视网膜、小脑和延髓血管母细胞瘤；肾囊肿和肾癌；胰腺囊肿；嗜铬细胞瘤；以及附睾乳头状囊腺瘤。我们报告了一例40岁患有I型冯·希佩尔-林道病的男性患者，其复发性小脑血管母细胞瘤接受了体外放射治疗。
