Published online Jan 27, 2025. doi: 10.4240/wjgs.v17.i1.98891
Revised: September 26, 2024
Accepted: November 18, 2024
Published online: January 27, 2025
Processing time: 171 Days and 23.6 Hours
Cystic lymphangioma is a rare hamartoma that is especially found in the adult gastrointestinal tract. In the early stage, most patients are asymptomatic; after the onset of symptoms, there is often no specificity regarding symptoms.
Here we report the endoscopic diagnosis and treatment of an adult patient with cystic lymphangioma of the ascending colon. One patient who came to our hospital with “dull pain in the left lower abdomen for 2 days” was initially misdiagnosed with a colon cyst according to endoscopy and then underwent endoscopic submucosal dissection. The final pathological results suggested cystic lymphangioma. One year later, no recurrence was found on re-examination via colonoscopy.
Cystic lymphangioma in the gastrointestinal tract rarely occurs in adults and is easily misdiagnosed or missed. Endoscopy, imaging, histology, and immunohistochemical staining are useful for diagnosis. Surgical resection is the preferred treatment.
Core Tip: We report an endoscopic diagnosis and treatment of cystic lymphangioma of the ascending colon in adults. Based on a literature review, we summarize the aetiology, symptoms, diagnosis, treatment, and prognosis of cystic lymphangioma. Because the lesion is located in the intestinal cavity, it is extremely rare, providing additional information and reference for future diagnosis and treatment of such cases.
