Cystic hemolymphangioma and jejunal duplication are both typically congenital conditions and primarily identified in childhood, making adult diagnoses exceedingly uncommon. Cystic hemolymphangioma and intestinal duplication together are particularly rare. In this report, we present the case of an adult female patient with both. A pedunculated mass was identified outside the jejunal wall, with duplicated intestine on the stalk and cystic hemolymphangioma within the mass. Both lesions were surgically excised, and the patient has remained recurrence-free for five years postoperatively.
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| http://dx.doi.org/10.7759/cureus.78197 | DOI Listing |
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A Rare Case of Cystic Hemolymphangioma Associated With Intestine Duplication.
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Article Synopsis
- - Gastrointestinal hemolymphangiomas, particularly in the rectum, are extremely rare, with only three diffuse cases documented in English literature, while this case presents the first localized version.
- - A 51-year-old woman with intermittent constipation was diagnosed through colonoscopy and imaging techniques, which revealed a mixed-echo mass and a cystic lesion between the rectum and vagina.
- - The patient underwent surgical removal of the lesions, confirmed as localized hemolymphangioma through pathological analysis, highlighting the importance of imaging in diagnosis and assessing lesion extent.
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