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先天性泄殖腔畸型－病例報告及文獻回顧
Congenital Cloacal Anomaly-Case Report and Literature Review
並列摘要
Congenital cloacal anomaly is a rare and complicated congenital malformation which requires surgical correction. We report a 5-year old girl with this anomaly who has suffered from stool incontinence due to a failed anorectoplasty at 1-year-old and frequent urinary tract infection, a well-knowledged complication associated with this anomaly. After review of all the reported experience in dealing with this anomaly, we successfully treat this girl with an planned one-stage reconstructive operation including vaginoplasty, re-do anorectoplasty and resection of vaginal septum with a cystoscope.
延伸閱讀
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