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与先天性袋状结肠相关的假性膀胱外翻。

Pseudoexstrophy associated with congenital pouch colon.

作者信息

Chadha R, Sharma A, Bagga D, Mahajan J K

机构信息

Department of Paediatric Surgery, Lady Hardinge Medical College and Kalawati Saran Children's Hospital, New Delhi, India.

出版信息

J Pediatr Surg. 1998 Dec;33(12):1831-3. doi: 10.1016/s0022-3468(98)90299-8.

Abstract

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.

摘要

假性膀胱外翻或隐匿性膀胱外翻是一种罕见的膀胱外翻变异型。作者报告了一例隐匿性膀胱外翻病例,该病例表现为新生儿耻骨和直肠肌肉广泛分离、脐低位以及皮下膀胱。肛门开口缺失,外生殖器存在复杂畸形,包括小的、向外侧移位的阴茎和右侧异位半阴囊。排尿和尿失禁正常。该患儿还患有高位肛门直肠畸形并伴有IV型先天性袋状结肠(CPC)畸形。双肾正常。初步手术包括在结肠袋近端行乙状结肠造口术。本文回顾了相关文献并讨论了假性膀胱外翻及其相关畸形的胚胎发生。

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