肛门直肠畸形伴直肠前庭瘘和阴道缺失:使用直肠膀胱瘘作为新阴道,然后进行保留肛门括约肌的 PSARP。

Pub Date : 2021-01-01 Epub Date: 2021-07-12 DOI:10.1055/s-0041-1728725
Antonio Dessanti, Osnel Louisma, Gabriel Steve Pierre, Nguhien Thanh Liem
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引用次数: 0

摘要

肛门直肠畸形、直肠前庭瘘伴有阴道发育不全的情况非常罕见。我们报告了一名在 1 岁时被确诊为这种合并症的患儿。在做了分段降结肠造口术后,我们选择保留直肠-直肠前庭瘘作为新阴道,同时通过改良的后矢状肛门成形术重新定位乙状结肠。结肠造口在主手术后 6 个月关闭。经过 3 年的随访,患者的大便和小便情况良好。新阴道的内口看起来很宽,易于探查。我们的结论是,我们的手术方法对这些儿童来说可能是一个不错的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anorectal Malformation with Rectovestibular Fistula and Vaginal Agenesis: Usage of Rectovestibular Fistula as a Neovagina Followed by PSARP with Preservation of the Anal Sphincter.

Anorectal Malformation with Rectovestibular Fistula and Vaginal Agenesis: Usage of Rectovestibular Fistula as a Neovagina Followed by PSARP with Preservation of the Anal Sphincter.

Anorectal Malformation with Rectovestibular Fistula and Vaginal Agenesis: Usage of Rectovestibular Fistula as a Neovagina Followed by PSARP with Preservation of the Anal Sphincter.

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Anorectal Malformation with Rectovestibular Fistula and Vaginal Agenesis: Usage of Rectovestibular Fistula as a Neovagina Followed by PSARP with Preservation of the Anal Sphincter.

Anorectal malformation with rectovestibular fistula associated with vaginal agenesis is rare. We report on a child in whom this combination was diagnosed at the age of 1 year. After creation of a divided descending colostomy, we chose to leave the rectum-rectovestibular fistula to function as a neovagina, while the sigmoid colon was relocated via modified posterior sagittal anorectoplasty. The colostomy was closed 6 months after the main surgery. After a follow-up of 3 years, the patient is continent for stool and urine. The introitus of the neovagina appears wide and easy to explore. We conclude that our surgical approach may be a good option for these children.

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