J Korean Assoc Pediatr Surg.
1995 Dec;1(2):190-194. 10.13029/jkaps.1995.1.2.190.
A Cloacal Exstrophy Variant Associated with Hindgut Duplication
- Affiliations
-
- 1Devision of Pediatric Surgery, College of Medicine, Kyung Hee University, Seoul, Korea.
- KMID: 2440249
- DOI: http://doi.org/10.13029/jkaps.1995.1.2.190
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.
Keyword
- Full Text Links
-
- Actions
-
Cited
- CITED
-
- Close
- Share
-
- Similar articles
-
- Initial Experiences of Complete Primary Exstrophy Repair in Cloacal and Bladder Exstrophy
- A case of congenital cloacal exstrophy/omphalocele-exstrophy-imperforate anus-spinal defects syndrome and a successful pregnancy
- The Experiences of Cloacal and Bladder Exstrophy: 3 Cases
- Analyzing the factors that contribute to the development of embryological classical type of bladder exstrophy
- Bladder Exstrophy with Successful Initial Closure
