| Literature DB >> 19589581 |
Yuya Nakano1, Madoka Aizawa, Sumie Honma, Yuichi Osa.
Abstract
A male infant born at 32 weeks of gestation and weighing 1.44 kg had penile agenesis, bifid scrotums, an anorectal anomaly, and suspected omphalocele. An operation revealed complete urethral agenesis, duplicated and blind bowels, a vesicointestinal fistula without exstrophy, and a urachal fistula; however, no omphaloceles were detected. To our knowledge, this is the first report on aphallia accompanied with completely separated scrotum and a vesicointestinal fistula without exstrophy; this condition is associated with urorectal septum malformation sequence (URSMS) and covered cloacal exstrophy. The possible embryogenesis is discussed in this study.Entities:
Mesh:
Year: 2009 PMID: 19589581 DOI: 10.1016/j.urology.2009.04.055
Source DB: PubMed Journal: Urology ISSN: 0090-4295 Impact factor: 2.649