Division of Urology, Centre Hospitalier Universitaire de Québec, Université Laval, Quebec, Canada.
Urology. 2011 Aug;78(2):431-3. doi: 10.1016/j.urology.2010.11.010. Epub 2011 Feb 5.
Persistent cloaca and caudal duplication are 2 rare anomalies of embryogenesis that can present with a wide variety of pelvic malformations. Here we present the rare case of a female born with both abnormalities. The infant was born with a single introitus, an imperforate anus, a didelphys uterus, a duplicated cervix and vagina, and accessory limb and coccyx. Multiple surgeries were performed to correct for the anomalies that would have otherwise had important health and lifestyle consequences for the child.
持续性泄殖腔和尾部重复是 2 种罕见的胚胎发育异常，可表现出多种骨盆畸形。我们在此报告了 1 例同时存在这 2 种异常的女性病例。该婴儿出生时有单个阴道入口、肛门闭锁、双子宫、宫颈和阴道重复、副肢和尾骨。为了纠正这些异常，进行了多次手术，否则这些异常会对孩子的健康和生活方式产生重要影响。
