一种不寻常的腹泻病因:原发性肠淋巴管扩张。

IF 4 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Cong Dai, Yu-Hong Huang
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引用次数: 0

摘要

原发性肠淋巴管扩张症(PIL)是一种罕见的疾病,其特征是肠淋巴管畸形和扩张,导致淋巴液引流受损和渗漏到胃肠道管腔。这会导致蛋白质丢失性肠病,引起慢性腹泻、外周水肿、体重减轻以及由于蛋白质、淋巴细胞和脂质丢失而导致的低白蛋白血症。在排除恶性肿瘤、手术或炎症等继发原因后,诊断依赖于内镜下典型白色粘膜斑块(代表淋巴扩张)的可视化和淋巴扩张的组织病理学证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An unusual etiology of diarrhea: primary intestinal lymphangiectasia.

Primary intestinal lymphangiectasia (PIL) is a rare disorder characterized by malformed and dilated intestinal lymphatic vessels, resulting in impaired drainage and leakage of lymph fluid into the gastrointestinal lumen. This leads to protein-losing enteropathy, causing chronic diarrhea, peripheral edema, weight loss, and hypoalbuminemia due to loss of proteins, lymphocytes, and lipids. Diagnosis relies on endoscopic visualization of pathognomonic white mucosal plaques (representing dilated lymphatics) and histopathological confirmation of lymphatic dilation, after excluding secondary causes like malignancy, surgery, or inflammatory conditions.

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来源期刊
CiteScore
2.00
自引率
25.00%
发文量
400
审稿时长
6-12 weeks
期刊介绍: La Revista Española de Enfermedades Digestivas, Órgano Oficial de la Sociedad Española de Patología Digestiva (SEPD), Sociedad Española de Endoscopia Digestiva (SEED) y Asociación Española de Ecografía Digestiva (AEED), publica artículos originales, editoriales, revisiones, casos clínicos, cartas al director, imágenes en patología digestiva, y otros artículos especiales sobre todos los aspectos relativos a las enfermedades digestivas.
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