Image of the Month: Clinical Features in a Newborn with Covered Cloacal Exstrophy

Author:

Vilanova-Sánchez Alejandra1,Ching Christina2,Gasior Alessandra3,Diefenbach Karen3,Wood Richard4,Levitt Marc4

Affiliation:

1. Department of Pediatric Surgery, Center for Colorectal and Pelvic Reconstruction, Nationwide Children's Hospital, Columbus, Ohio, United States

2. Department of Pediatric Urology, Nationwide Children's Hospital, Columbus, Ohio, United States

3. Department of Pediatric Surgery, Nationwide Children's Hospital, Columbus, Ohio, United States

4. Center for Colorectal and Pelvic Reconstruction, Nationwide Children's Hospital, Columbus, Ohio, United States

Abstract

AbstractCloacal exstrophy is the most severe type of anorectal malformations that belongs to the bladder–exstrophy–epispadias complex of genitourinary malformations. Interestingly, its variant, the covered cloacal exstrophy, is often missed. The clinical findings of this variant may include an imperforate anus, low lying umbilicus, thick pubic bone, and pubic diastasis but with an intact abdominal wall. We present an interesting case of covered cloacal exstrophy with a side-by-side duplicated bladder and discuss important considerations for the time of colostomy creation in the newborn period.

Publisher

Georg Thieme Verlag KG

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