女性双尿道：一例报告。
Female double urethra: a case report.
机构信息
Hamad Medical Corporation, Doha, Qatar.
出版信息
J Pediatr Surg. 2012 Aug;47(8):e29-31. doi: 10.1016/j.jpedsurg.2012.04.006.
Abstract
Female double urethra is a very rare anomaly, with less than 40 cases reported since 1970. Most reported cases of double urethra are in the sagittal plane and tend to be stenotic. We describe a 4-year-old girl with double urethra, which was not stenotic and was in the coronal plane. Double urethra should be excluded among other causes in any girl who is incontinent beyond the continence age.
摘要
女性双尿道是一种非常罕见的异常，自 1970 年以来，报道的病例不到 40 例。大多数报道的双尿道病例位于矢状面，且往往存在狭窄。我们描述了一例 4 岁女孩的冠状面非狭窄性双尿道病例。对于任何超过控尿年龄仍出现尿失禁的女孩，应排除其他病因后考虑双尿道。
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