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患有贝克威思-维德曼综合征的儿童出现髓质海绵肾和单侧肾母细胞瘤。

Medullary sponge kidneys and unilateral Wilms tumour in a child with Beckwith-Wiedemann syndrome.

作者信息

Beetz R, Schofer O, Riedmiller H, Schumacher R, Gutjahr P

机构信息

Department of Paediatrics, University Hospital, Mainz, Federal Republic of Germany.

出版信息

Eur J Pediatr. 1991 May;150(7):489-92. doi: 10.1007/BF01958430.

Abstract

The occurrence of a Wilms tumour in a 4-year-old girl with bilateral medullary sponge kidney. Beckwith-Wiedemann syndrome and congenital hemihypertrophy demonstrates the close relationship between these disorders. Another six cases from the literature with congenital hemihypertrophy and with medullary sponge kidney are discussed, two of them also developed intraabdominal neoplasm.

摘要

一名患有双侧髓质海绵肾、贝克威思-维德曼综合征和先天性半侧肥大的4岁女孩发生了肾母细胞瘤,这表明了这些病症之间的密切关系。文中还讨论了另外6例先天性半侧肥大并伴有髓质海绵肾的病例,其中2例也发生了腹内肿瘤。

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