Watanabe Y, Todani T, Fujii T, Toki A, Uemura S, Koike Y
Z Kinderchir. 1985 Apr;40(2):114-6. doi: 10.1055/s-2008-1059729.
A high incidence of congenital malformations with Wilms' tumor had been recognized lately. Aniridia, hemihypertrophy, chromosome deletion, urinary tract anomalies, and Wiedemann-Beckwith syndrome have often been observed in patients with Wilms' tumor. However, Wilms' tumor associated with Moyamoya disease, which refers to a stenosis of the distal portion of the carotid artery with an abnormal network in the brain base, has never been reported. In this report, a male child aged 28 mo. with Wilms' tumor associated with Moyamoya disease is presented.
近来已认识到肾母细胞瘤合并先天性畸形的发生率很高。无虹膜、半身肥大、染色体缺失、泌尿系统异常以及威德曼-贝克威思综合征常可见于肾母细胞瘤患者。然而，肾母细胞瘤合并烟雾病（指颈动脉远端狭窄伴脑底部异常血管网）的情况此前从未有过报道。在本报告中，我们介绍了一名28个月大的男性儿童，其患有肾母细胞瘤合并烟雾病。
