ArticleCureus2026
Small Bowel Lymphangiomatosis Presenting With Amyloidosis: A Case Report.
Article in Cureus, 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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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Small bowel lymphangiomatosis is a rare benign lymphatic malformation with nonspecific clinical manifestations that may complicate preoperative diagnosis. We present the case of a 57-year-old male with a history of recurrent umbilical hernias who complained of abdominal pain, nausea, vomiting, and an unreducible ventral hernia, all of which suggested a small bowel obstruction. Imaging revealed a presumed strangulated hernia with bowel obstruction and abnormal thickening of various loops of small bowel. Exploratory laparotomy disclosed incarcerated and gangrenous small bowel requiring resection. Histopathologic evaluation demonstrated extensive small-bowel lymphangiomatosis with concurrent AA-dominant amyloidosis, confirmed by apple-green birefringence on polarized microscopy of a Congo red-stained sample. This case highlights a rare coexistence of lymphangiomatosis and amyloidosis and suggests a possible relationship between chronic inflammatory amyloid deposition and secondary lymphatic obstruction, which may contribute to lymphangioma formation.
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