ArticleACG case reports journal2026
Abdominal Lymphatic Malformations Presenting as Protein-Losing Enteropathy.
Article in ACG case reports journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
3 authors.
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Abstract
Lymphatic malformations (LMs), previously known as lymphangiomas, are rare, benign tumors characterized by abnormal proliferation of lymphatic vessels. They are common in the neck and axilla. Abdominal LMs are exceedingly rare. Clinically, abdominal LMs are often asymptomatic and discovered incidentally on imaging. The following case presents a young female whose diagnosis of abdominal LMs was associated with chronic diarrhea, weight loss, and intermittent edema. Nearly all LMs are treated surgically. Upon literature review, this is the first case of an adult with abdominal LMs causing protein-losing enteropathy that was treated with dietary changes alone.
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