Gupta Sandeep, Kumar Barun, Basu Sandip, Pal Dilip Kumar
Department of Urology, Institute of Post Graduate Medical Education and Research Kolkata, Kolkata, India.
Department of Plastic Surgery, Institute of Post Graduate Medical Education and Research, Kolkata, India.
BMJ Case Rep. 2017 Jul 24;2017:bcr-2017-221198. doi: 10.1136/bcr-2017-221198.
We report a case of 21-year-old young woman with congenital cloacal malformation. She was operated at the age of 1.5 years separating the rectum from common opening as a two-stage repair. She was incontinent in the earlier part of her life but she became continent to some extent later in early adulthood. She presented with urinary stress incontinence following delivery of dead fetus of 6 months. She underwent multiple investigations revealing common opening of bladder neck and vagina. A multidisciplinary evaluation was done and she underwent closure of common channel and neourethra reconstruction using pedicled appendix. Patient was continent and voiding by herself on discharge.
我们报告一例21岁先天性泄殖腔畸形的年轻女性病例。她在1.5岁时接受手术,分两期将直肠与共同开口分离进行修复。她早年大小便失禁,但在成年早期后来在一定程度上实现了自控。她在流产6个月大的死胎后出现了压力性尿失禁。她接受了多项检查,发现膀胱颈和阴道有共同开口。进行了多学科评估,她接受了共同通道闭合术,并使用带蒂阑尾进行了新尿道重建。患者出院时能够自行控制排尿。