| Literature DB >> 22170701 |
Toshihiro Yanai1, Yasuhisa Urita, Teruyoshi Amagai, Hajime Kawakami, Hiroko Watayo, Takayuki Masuko, Satoshi Matsuda, Misako Hirai, Toshihiro Muraji, Hiromi Hamada.
Abstract
Cloacal dysgenesis sequence (CDS) is a rare and lethal malformation. We report such a case of long-term survival, currently to 12 years of age. In the fetal period, she received a timely placement of vesico-amniotic shunt for a megabladder due to a severe urethral obstruction. Postnatally, cystostomy and colostomy were created because of no perineal opening of urethra, vagina, and anus. Anorectoplasty, construction of efferent conduit, and colostomy closure were performed at 4 years of age. Ileovaginoplasty and ileovesicostomy which was a Mitrofanoff-type of conduit, and labioplasty were performed at the age of 11 years. To the best of our knowledge, only five survivors with CDS over 1 year of age have been reported.Entities:
Mesh:
Year: 2012 PMID: 22170701 DOI: 10.1007/s00383-011-3020-3
Source DB: PubMed Journal: Pediatr Surg Int ISSN: 0179-0358 Impact factor: 1.827