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Updated: Aug 30, 2025

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
Published on: May 1, 2015
Jejunal lymphangioma
1Endoscopy, University of the Ryukyus, Japan.
This case report details a jejunal lymphangioma, a rare condition presenting as cystic masses in the small intestine. Diagnosis involved CT scans, enteroscopy, and histopathology confirming dilated lymphatic channels.
Area of Science:
- Gastroenterology
- Pathology
- Surgical Oncology
Background:
- Intestinal lymphangioma is a rare benign tumor originating from the lymphatic system.
- It can present with various symptoms depending on the location and size.
- Accurate diagnosis is crucial for appropriate management.
Observation:
- A patient presented with non-enhancing cystic masses in the jejunum identified via CT scan.
- Enteroscopy revealed multiple cystic swellings with characteristic whitish, carpet-like villi.
- Histopathological examination confirmed dilated lymphatic channels lined by endothelial cells.
Findings:
- Immunohistochemical staining was positive for lymphatic endothelial markers, confirming the diagnosis.
- The findings are consistent with a primary jejunal lymphangioma.
- This highlights the utility of combined imaging and endoscopic evaluation.
Implications:
- This case contributes to the understanding of jejunal lymphangioma presentation and diagnosis.
- Early and accurate diagnosis can guide surgical or conservative management strategies.
- Further research into the pathogenesis and optimal treatment of intestinal lymphangiomas is warranted.
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