All issues > Volume 31(3); 1988
- Original Article
- J Korean Pediatr Soc. 1988;31(3):404-409. Published online March 31, 1988.
- A Case of Cloacal Extrophy.
- Byung Ho Lee1, Soon Seon Lim1, Young Ha Kim1, Moon Ki Cho1
- 1Department of Pediatrics, Saint Columbanban Hospital, Mokpo, Korea
- Received: October 13, 1987;
- Abstract
- Cloacal exstrophy is an extremly rare and curious anomaly that involves not only the genitourinary
system but also the intestinal tract, resulted from the abnormaly large cloacal membrane and its early
dehiscence.
The authors experienced a case of cloacal exstrophy in one day old neonate whose intestine and
bladder were exstrophied and showed omphalocele, imperforated anus and meningocele.
Radiologic examination revealed widely separated symphysis pubic bone and spina bifida.
A brief review of related literatures was made.
Keywords :Cloacal Exstrophy