Pseudoexstrophy associated with congenital pouch colon

被引:12
作者
Chadha, R
Sharma, A
Bagga, D
Mahajan, JK
机构
[1] Lady Hardinge Med Coll, Dept Paediat Surg, New Delhi 110001, India
[2] Kalawati Saran Childrens Hosp, New Delhi 110001, India
关键词
bladder exstrophy; exstrophy variants; pseudoexstrophy; covered exstrophy; anorectal malformations; scrotal abnormalities;
D O I
10.1016/S0022-3468(98)90299-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Pseudoexstrophy or covered exstrophy is a rare exstrophy variant. The authors report a case of covered exstrophy that presented as a newborn with widely separated pubic bones and rectus muscles, a low-set umbilicus, and a subcutaneous bladder. The anal opening was absent, and there was a complex malformation of the external genitalia consisting of a small, laterally displaced penis and a right-sided ectopic hemiscrotum. Micturition and urinary continence were normal. The child also had a high anorectal malformation with a coexistent type IV congenital pouch colon (CPC) malformation. Both kidneys were normal. Preliminary surgery consisted of a divided sigmoid colostomy proximal to the colonic pouch. The literature is reviewed and the embryogenesis of pseudoexstrophy and its associated malformations are discussed. J Pediatr Surg 33:1831-1833. Copyright (C) 1998 by W.B. Saunders Company.
引用
收藏
页码:1831 / 1833
页数:3
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