Anomalous congenital band causing duodenal and transverse colon obstruction in a 3-year-old girl: A case report

IF 0.2 Q4 PEDIATRICS
Amnah Fallatah , Muhammad Afzal , Sania Alblushi , Zeinab Alsulaiman , Huda Hussain Abugrain , Ahmed Tabash
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Abstract

Introduction

Intestinal obstruction is commonly seen in children and may result from various acquired or congenital causes. Obstruction due to an anomalous congenital band (ACB) is exceptionally rare. These bands can develop anywhere along the gastrointestinal tract and often pose a diagnostic challenge preoperatively.

Case presentation

A 3-year-old girl presented with chronic constipation, abdominal pain, and bilious vomiting. She was initially diagnosed and treated for conditions such as simple constipation, cystitis, enteritis, and gastritis, but showed no improvement. The radiological evaluation included abdominal radiography, ultrasound, dual-contrast computed tomography (CT), and a single-contrast enhanced image of the upper gastrointestinal tract (GIT). Surgical intervention was undertaken based on CT and upper GIT contrast imaging findings indicating an obstruction in the second part of the duodenum. Operative findings revealed an ACB arising from the root of the small intestinal mesentery, obstructing both the duodenum and the transverse colon. The band was divided, and a portion of it was sent for histopathological examination. The postoperative period was uneventful, her symptoms fully resolved, and she was discharged on the 6th postoperative day. At the 2-month follow-up, she remained asymptomatic. To our knowledge, no such case has previously been documented in the literature.

Conclusion

Anomalous congenital bands should be considered in the differential diagnosis of children presenting with intestinal obstruction in the absence of previous abdominal operations, particularly when preoperative imaging findings are inconclusive.
异常先天性束带致3岁女童十二指肠及横结肠梗阻1例
肠梗阻常见于儿童,可由各种后天或先天性原因引起。异常先天性带梗阻(ACB)是非常罕见的。这些条带可以沿着胃肠道的任何地方出现,并且经常对术前诊断构成挑战。病例表现:一名3岁女童,慢性便秘、腹痛、胆汁性呕吐。她最初被诊断为单纯性便秘、膀胱炎、肠炎和胃炎,但没有任何改善。放射学评估包括腹部x线片、超声、双对比计算机断层扫描(CT)和单对比增强上胃肠道图像(GIT)。根据CT和上消化道造影显示十二指肠第二部分梗阻,采取手术干预。手术结果显示,ACB起源于小肠肠系膜根部,阻塞了十二指肠和横结肠。将带子切开,取一部分送组织病理检查。术后顺利,患者症状完全缓解,于术后第6天出院。在2个月的随访中,她仍然无症状。据我们所知,以前文献中没有记录过这样的病例。结论对未做过腹部手术的肠梗阻患儿,尤其是术前影像学表现不明确的患儿,应考虑先天性带异常的鉴别诊断。
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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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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