一名患有丹迪-沃克综合征的儿童出现双侧囊性肾母细胞瘤和葡萄状肉瘤。
Bilateral cystic nephroblastomas and botryoid sarcoma in a child with Dandy-Walker syndrome.
作者信息
Kinoshita T, Nakamura Y, Kinoshita M, Fukuda S, Nakashima H, Hashimoto T
出版信息
Arch Pathol Lab Med. 1986 Feb;110(2):150-2.
PMID:3004372
Abstract
We report an autopsy case of an 8-month-old male infant with bilateral cystic nephroblastomas, a botryoid sarcoma involving the urinary bladder, microencephaly, the Dandy-Walker syndrome, bilateral cataracts, hypospadias, and male pseudohermaphroditism. An unusual combination of congenital malformation and tumors may reflect the presence of a mutant gene.
摘要
我们报告一例8个月大男婴的尸检病例，该患儿患有双侧囊性肾母细胞瘤、累及膀胱的葡萄状肉瘤、小头畸形、丹迪-沃克综合征、双侧白内障、尿道下裂和男性假两性畸形。先天性畸形与肿瘤的异常组合可能反映了突变基因的存在。
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