CASE REPORT
A Case of Ultra-High Rectovaginal Fistula after Sex Reassignment Surgery
Akihiro Toyosaka, Naoyuki Murata, Yasuhiro Mishima, Tatsuya Andoh, Suguru Ohmuro, Yasuji Seki1) and Hiromichi Kanehiro2)
Department of Surgery, Takarazuka-Daiichi Hospital
Seki Children's Clinic1)
Department of Surgery, Nara Medical University2)
We report a rare case of rectovaginal fistula (RVF) after sex reassignment surgery (SRS) in a 33-year-old male-to-female transsexual. Having undergone SRS 7 years earlier, she had been treated elsewhere 3 years earlier for fecal discharge and bleeding from the neovagina. Contrast enema and endoscopy showed an ultra-high RVF of the rectosigmoid portion, necessitating sigmoid colostomy immediately after admission. Repair of the RVF by a transsacral approach from outside of the rectum was conducted 2 months later. The RVF was successfully closed but with difficulty due to severe intrapelvic adhesion. The colostomy was closed 2 months later. The patient has been problem-free in the 1 year and 3 months since repair. The cause of the RVF was thought to be obturator decubitus due to long-term continuous intravaginal stenting. Vaginal function has not been restored because the patient fears recurrence. We know of no reports of treatment by local repair with a transsacral approach for extremely high RVF of the rectosigmoid portion.
Key words
sex reassignment surgery, rectovaginal fistula, transsacral approach
Jpn J Gastroenterol Surg 42: 417-423, 2009
Reprint requests
Akihiro Toyosaka Department of Surgery, Takarazuka-Daiichi Hospital
19-5 Kougetsu-cho, Takarazuka, 665-0832 JAPAN
Accepted
October 22, 2008
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