Complete Colonic Duplication and Perineal Fistula: Transanal Mucosectomy of the Ectopic Rectum.

Pub Date : 2022-08-16 eCollection Date: 2022-01-01 DOI:10.1055/s-0042-1750028
Johannes W Duess, Peter Zimmermann, Franz W Hirsch, Daniel Graefe, Martin Lacher, Jan-Hendrik Gosemann
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Abstract

Background Colonic duplication may present in different anatomic variants. The surgical approach towards these anomalies can be challenging and has implications for subsequent future continence. Case Description  We report on a 1-year-old girl with congenital heart defect and pacemaker who was referred to us with an anorectal malformation. The patient was stooling from both an anus and a perineal fistula. Examination under anesthesia revealed an orthotopic and age-appropriate sized anus with surrounding sphincter and a second rectal lumen ending as a perineal fistula. A computed tomography and contrast enema indicated colonic duplication. Exploratory laparotomy showed a duplicated terminal ileum leading to two ceca and appendices, which joined to a duplicated colon with a septum and common mesentery. At the rectosigmoid junction, one part of the duplication ended as a perineal fistula, the second one led to the (orthotope) anus. The common colonic wall was divided using a stapler. The rectal duplication leading to the perineal fistula was not completely resected but treated by mucosectomy only (Soave plane) leaving its muscular cuff in place. Finally, an ileostomy was created. The postoperative course was uneventful. A contrast enema prior to ostomy takedown demonstrated a well-configurated colon and rectum without stenosis or impaction. The girl is currently continent with a complete resolution of her constipation. Conclusion  In cases of complete colonic duplication division of the common wall is simple and safe. Mucosectomy of the ectopic rectum limits pelvic dissection and preserves the entire muscular wall of the duplicated orthotope rectum.

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完全结肠复制和会阴瘘:经肛门粘膜切除术治疗异位直肠。
背景结肠复制可能出现在不同的解剖变异中。手术治疗这些异常可能具有挑战性,并对后续的尿失禁有影响。病例描述我们报告一个1岁的女孩先天性心脏缺陷和起搏器谁是转介到我们的肛门直肠畸形。患者同时从肛门和会阴瘘管处大便。麻醉下的检查显示一个正位和年龄大小的肛门,周围有括约肌和第二直肠管,末端为会阴瘘管。计算机断层扫描和灌肠造影显示结肠复制。剖腹探查显示重复的回肠末端通向两个盲肠和阑尾,并与重复的结肠、隔和总肠系膜相连。在直肠乙状结肠连接处,重复的一部分作为会阴瘘管结束,另一部分通向(正位)肛门。用订书机将普通结肠壁分开。导致会阴瘘管的直肠复制未完全切除,但仅行粘膜切除术(Soave平面),保留其肌肉袖带。最后,进行回肠造口术。术后过程平淡无奇。造口术前的对比灌肠显示结肠和直肠结构良好,没有狭窄或嵌塞。这个女孩的便秘现在已经完全解决了。结论在完全结肠复制病例中,分离共壁是一种简单、安全的方法。异位直肠的粘膜切除术限制了盆腔剥离,并保留了复制直直肠的整个肌壁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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