Herman T E, Coplen D, Skinner M
Department of Radiology, Mallinckrodt Institute of Radiology, St. Louis Children's Hospital, MO 63110, USA.
Pediatr Radiol. 2000 Apr;30(4):243-6. doi: 10.1007/s002470050730.
We report a case of a persistent cloaca and pseudoexstrophy associated with congenital pouch colon in a native-born American female child. This unusual anomaly occurs in two clinical settings. It has been reported in India as an isolated anomaly occurring primarily in males. Pouch colon also occurs in female patients with pseudoexstrophy or closed cloacal exstrophy. The typical anatomic features of this anomaly are discussed.
我们报告了一例美国本土出生的女童，其患有持续性泄殖腔和假性膀胱外翻，并伴有先天性袋状结肠。这种不寻常的异常情况出现在两种临床情形中。在印度，它被报告为一种主要发生在男性中的孤立性异常。袋状结肠也见于患有假性膀胱外翻或闭锁性泄殖腔外翻的女性患者。本文讨论了这种异常的典型解剖特征。
