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伴有异位胃黏膜和肛门狭窄的肛管重复畸形:首例病例报告及文献综述

Anal canal duplication with heterotopic gastric mucosa and anal stenosis: first case report and literature review.

作者信息

Liu Chen, Xu Chuanzhen, Xu Xiaoliang, Zhang Yan, Geng Lei, Mei Yanhui, Ji Hong, Fu Tingliang, Ding Guojian

机构信息

Department of Surgery, Shanghai Children's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

Department of Pediatric Surgery, Binzhou Medical University Hospital, Binzhou, Shandong, China.

出版信息

Front Pediatr. 2024 Sep 5;12:1452116. doi: 10.3389/fped.2024.1452116. eCollection 2024.

Abstract

INTRODUCTION

Anal canal duplication (ACD) is a rare entity of gastrointestinal duplication that may be asymptomatic or present complications, such as abscess, fistulae, or malignant changes. The diagnosis and rational management of ACD still need to be clarified.

CASE PRESENTATION

We present a case of an 18-month-old girl with intractable perianal erosion and painful bowel movements for one year, and chronic constipation for six months. Fistulography revealed a tubular structure (3 cm in length), located posterior to the native anal canal. Mucosectomy was performed through a perineal approach combined with a coccigeal approach, and the postoperative course was uneventful. The pathological findings confirmed the diagnosis of ACD with heterotopic gastric mucosa, a rare combination that has not been described in the literature before. A literature search was conducted on the Medline database for studies reporting ACD in children. The study pool consisted of 77 cases of ACD from 32 studies, including the present case. According to our case report and in line with the literature, 43 cases (55.84%) were incidentally found; the most frequent symptom was constipation (14.29%), followed by painful anal mass or sacral pain (10.39%), and recurrent fistula (7.79%). Coexisting diseases were observed in 31 patients (40.26%), including 19 (24.68%) cases associated with presacral masses. Surgical management was employed in 73 patients (94.81%). ACD excision was performed in 47 patients (64.38%), combined with presacral mass resection or coccygectomy in 19 cases (26.03%).

CONCLUSION

Preoperative imaging, including fistulography, ultrasonography, and magnetic resonance imaging, can provide useful information, especially for screening its associated anomalies. To prevent potential complications, surgical removal of ACD and associated anomalies is recommended. Mucosectomy may be one of the most effective surgical options for ACD due to its excellent functional outcome.

摘要

引言

肛管重复畸形(ACD)是一种罕见的胃肠道重复畸形,可能无症状,也可能出现脓肿、瘘管或恶性病变等并发症。ACD的诊断和合理治疗仍需明确。

病例报告

我们报告一例18个月大的女童,顽固性肛周糜烂伴排便疼痛1年,慢性便秘6个月。瘘管造影显示一个管状结构(长3厘米),位于肛管后方。通过会阴联合尾骨入路进行了黏膜切除术,术后过程顺利。病理结果证实为伴有异位胃黏膜的ACD,这是一种罕见的组合,此前文献中未见描述。在Medline数据库中进行了文献检索,以查找报告儿童ACD的研究。研究组包括来自32项研究的77例ACD病例,包括本病例。根据我们的病例报告并结合文献,43例(55.84%)为偶然发现;最常见的症状是便秘(14.29%),其次是肛门肿物疼痛或骶骨疼痛(10.39%),以及复发性瘘管(7.79%)。31例患者(40.26%)存在合并疾病,其中19例(24.68%)与骶前肿物有关。73例患者(94.81%)采用了手术治疗。47例患者(64.38%)进行了ACD切除术,其中19例(26.03%)联合骶前肿物切除术或尾骨切除术。

结论

术前影像学检查,包括瘘管造影、超声和磁共振成像,可提供有用信息,尤其是用于筛查其相关异常。为预防潜在并发症,建议手术切除ACD及相关异常。由于其良好的功能结局,黏膜切除术可能是ACD最有效的手术选择之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/106d/11410600/a12c952aeba2/fped-12-1452116-g001.jpg

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