Department of General Surgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, China, No.56 Nanlishi St, Xicheng District, Beijing, 100045, China.
Department of Neonatal Surgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, China, No.56 Nanlishi St, Xicheng District, Beijing, 100045, China.
Pediatr Surg Int. 2022 Dec 2;39(1):31. doi: 10.1007/s00383-022-05316-7.
Alimentary tract duplication involving the rectum (ATD-R) is rare. The purpose of the study was to describe the features of pediatric ATD-R patients and propose a surgical management strategy.
Nine consecutive children operated on for ATD-R at a tertiary center for pediatrics from January 2010 to June 2021 were retrospectively reviewed and followed up. Eighty-six children with the same diagnosis from the literature were reviewed to assist the investigation. Classifications of ATD-R consisted of cystic, tubular, and diverticular.
Surgical treatment and histopathological examination identified six females and three males with ATD-R. Initial clinical symptoms included perianal lesions, abnormal discharge, and anorectal malformation (ARM). Apart from one tubular ATD-R patient with cloaca malformation, the other eight patients had normal-developed anorectum. Complete or partial lesion resection maintaining the integrity of the proper colorectum was a principle of surgery. Six patients were followed up for a median time of 71 (range 12-121) months with good prognoses. A surgical management strategy of ATD-R in children was proposed.
ATD-R commonly occurred concurrently with normal-developed anorectum, seldom combined with ARM. ATD-R should be considered as a differential diagnosis in anorectal symptoms. The timely and appropriate operation was curative.
涉及直肠的消化道重复畸形(ATD-R)较为罕见。本研究旨在描述儿科 ATD-R 患者的特征,并提出一种手术治疗策略。
回顾性分析 2010 年 1 月至 2021 年 6 月在一家儿科三级中心接受 ATD-R 手术的 9 例连续患儿,并进行随访。同时回顾了文献中 86 例具有相同诊断的患儿以协助调查。ATD-R 的分类包括囊性、管状和憩室状。
手术治疗和组织病理学检查确定了 6 名女性和 3 名男性患有 ATD-R。首发临床症状包括肛门周围病变、异常分泌物和肛门直肠畸形(ARM)。除了 1 例伴有泄殖腔畸形的管状 ATD-R 患者外,其余 8 例患者的肛门直肠发育正常。保留完整直肠的完整或部分病变切除是手术的原则。6 例患者获得了中位时间为 71 个月(范围 12-121 个月)的随访,预后良好。提出了一种儿童 ATD-R 的手术治疗策略。
ATD-R 通常与正常发育的肛门直肠同时发生,很少与 ARM 合并。在出现肛门直肠症状时应考虑 ATD-R 作为鉴别诊断。及时、适当的手术是可治愈的。