A Cloacal Exstrophy Variant Associated with Hindgut Duplication
10.13029/jkaps.1995.1.2.190
- Author:
Tae Seok LEE
1
;
Sao Myung OH
Author Information
1. Devision of Pediatric Surgery, College of Medicine, Kyung Hee University, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
Complete diphallus;
Displacement of bladder;
Hindgut duplication;
Imperforate anus;
Cloacal exstrophy
- MeSH:
Anus, Imperforate;
Cloaca;
Korea;
Male;
Penis;
Urinary Bladder;
Urinary Tract
- From:Journal of the Korean Association of Pediatric Surgeons
1995;1(2):190-194
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Diphallus is a rare congenital anomaly and is frequently associated with duplication of the urinary tract and rectosigmoid, and commonly associated with vertebral anomalies. Remzi reported less than 100 cases of duplication of all or a portion of the penis, but about 10 cases of complete diphallus with exstrophy of cloaca was reported, and a case of complete diphallus associated with hingut duplication was reported, and complete diphallus with displacement of bladder associated hindgut duplication and imperforate anus was not reported in Korea. We experienced a case of the complete diphallus associated with displacement of bladder, hindgut duplication, and imperforate anus as a variant of cloacal exstrophy. A review of published cases suggests that this may be the first example of a complete dip hall us with displacement of bladder coexisting with the hindgut duplication and imperforate anus.
