Primary intestinal lymphangiectasia presenting with intussusception in a child.

Q3 Medicine
Pediatria Medica e Chirurgica Pub Date : 2026-02-02 Epub Date: 2026-02-10 DOI:10.4081/pmc.2026.366
Kavita Gaur, Mukul Choudhary, Smita Singh, Kiran Agarwal, Abu Suraih, Subhasis Roy Choudhary
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引用次数: 0

Abstract

Intestinal lymphangiectasia is a protein losing intestinal disease caused by congenital malformation or obstruction of intestinal lymphatics. Based on etiology, it is classified as primary or secondary. Primary Intestinal Lymphangiectasia (PIL) is a rare disorder of intestinal lymphatic dysfunction and may present with a wide spectrum of clinical manifestations but it very infrequently presents as intussusception in children. To the best of our knowledge this is the second only reported case in children, both cases being described from the Indian subcontinent. A 12-year-old male presented complaining of abdominal pain for one week. Examination revealed a palpable mass in the right upper quadrant and abdominal tenderness. A provisional diagnosis of acute intestinal obstruction was made and the child underwent an emergency laparotomy which revealed a segment of distal ileum displaying intussusception. On cut opening, no growth was seen. Histopathology of the telescoped segment showed many ectatic and dilated lymphatic channels filled with lymph. PIL should be considered in the differential diagnosis in children presenting with intestinal obstruction.

儿童原发性肠淋巴管扩张,表现为肠套叠。
肠淋巴管扩张症是由肠淋巴管先天畸形或梗阻引起的一种蛋白质丢失性肠道疾病。根据病因,分为原发性和继发性。原发性肠淋巴管扩张症(PIL)是一种罕见的肠淋巴功能障碍疾病,可表现为广泛的临床表现,但在儿童中很少表现为肠套叠。据我们所知,这是报告的第二例儿童病例,这两例均来自印度次大陆。一名12岁男性主诉腹痛一周。检查发现右上腹有可触及的肿块和腹部压痛。初步诊断为急性肠梗阻,患儿接受紧急剖腹手术,发现回肠远端出现肠套叠。切开后,未见生长。伸缩节段的组织病理学显示许多扩张和扩张的淋巴通道充满淋巴。小儿肠梗阻的鉴别诊断应考虑PIL。
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
Pediatria Medica e Chirurgica
Pediatria Medica e Chirurgica Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.70
自引率
0.00%
发文量
21
审稿时长
10 weeks
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