Intraoperative diagnosis of rare pediatric internal hernias: A case series

IF 0.2 Q4 PEDIATRICS
Spencer E. Kim , William R. Johnston , Rosa Hwang , Gary W. Nace
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Abstract

Introduction

Internal hernias are a rare but serious condition in pediatric patients. Even with a thorough preoperative imaging workup, distinguishing them from other causes of bowel obstruction is challenging. This case series presents three patients with internal hernias of varying etiologies and complexity that were not diagnosed until intraoperative exploration.

Case series

Case 1 is a previously healthy 11-year-old boy with new-onset abdominal pain and emesis who was found to have a strangulated segment of small bowel herniated through a small congenital mesenteric defect. Case 2 is a 3-year-old boy with constipation presenting with acute-on-chronic abdominal pain. He was found to have a hernia sac formed from an abnormal attachment of omentum to the retroperitoneum, which contained segments of small and large bowel. Case 3 is a 23-year-old female with ataxia-telangiectasia-like syndrome and dystonia with a gastrostomy tube who presented with emesis and reflux. Surgical exploration revealed a highly unusual internal hernia through the hepatoduodenal and transverse mesocolon, through which the entire small bowel and majority of the transverse colon were herniated. None of these internal hernias were diagnosed with preoperative imaging. All patients underwent successful internal hernia repair with resolution of abdominal symptoms and have not required additional surgical workup.

Conclusion

Frequently, the diagnosis of an internal hernia is difficult to define preoperatively and is only made at the time of surgical exploration. Although internal hernias are rare, they should remain on the differential in pediatric and young adult patients presenting with signs of acute and/or chronic bowel obstruction.
罕见小儿内疝的术中诊断:一个病例系列
腹内疝是一种罕见但严重的儿科疾病。即使进行了彻底的术前影像学检查,将它们与其他原因的肠梗阻区分开来也是一项挑战。本病例系列介绍了三例不同病因和复杂性的内疝患者,直到术中探查才诊断出来。病例系列病例1是一名健康的11岁男孩,新发腹痛和呕吐,发现小肠绞窄部分通过一个小的先天性肠系膜缺陷疝出。病例2是一个3岁的男孩,便秘表现为急性慢性腹痛。他被发现有一个疝囊,由网膜与腹膜后的异常附着形成,腹膜后含有小肠和大肠的部分。病例3是一名23岁女性,患有共济失调-毛细血管扩张样综合征和肌张力障碍伴胃造瘘管,表现为呕吐和反流。手术探查发现一罕见的经肝十二指肠及横肠系膜的内疝,整个小肠及大部分横结肠均疝出。这些内疝均未通过术前影像学诊断。所有患者均成功进行了腹内疝修复,腹部症状得到缓解,不需要额外的手术检查。结论腹内疝的诊断往往在术前难以确定,只能在手术探查时才能确定。虽然腹内疝是罕见的,他们仍然应该在儿科和年轻的成人患者表现出急性和/或慢性肠梗阻的迹象的区别。
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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