ArticleWorld journal of gastroenterology2013
A case of colon perforation due to enteropathy-associated T-cell lymphoma.
Article in World journal of gastroenterology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 15 citations in OpenAlex.
- Intestinal T-cell lymphoma presenting as colonic perforation in the setting of ulcerative colitis: a case report.Clinical journal of gastroenterology · 2021Article
- Multiple cerebral lesions in a patient with refractory celiac disease: A case report.World journal of gastroenterology · 2020Article
- Monomorphic Epitheliotropic Intestinal T cell Lymphoma: a Rare Cause of Chronic Diarrhea.Journal of gastrointestinal cancer · 2019Article
- Multiple lesions of gastrointestinal tract invasion by monomorphic epitheliotropic intestinal T-cell lymphoma, accompanied by duodenal and intestinal enteropathy-like lesions and microscopic lymphocytic proctocolitis: a case series.Diagnostic pathology · 2016Article
- Enteropathy associated T-cell lymphoma presenting with multiple episodes of small bowel haemorrhage and perforation.Journal of surgical case reports · 2014Article
- Various Endoscopic Features in Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma.Case reports in gastroenterologyArticle
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Authors and funding
10 authors at 1 institution in 1 country.
Funding
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Abstract
Enteropathy-associated T-cell lymphoma (EATL) is an extremely rare disease, which is often related to gluten-sensitive enteropathy. It is an uncommon intestinal lymphoma with very poor prognosis and high mortality rate. In the absence of specific symptoms or radiological findings, it is difficult to diagnose early. Major complications of EATL have been known as intestinal perforation or obstruction, and only 5 cases of EATL are reported in South Korea. In this study, we report a case of 71-year-old male with symptoms of diarrhea, which later it progressed into cancer perforation of the colon. The initial colonoscopic findings were normal and computed tomography scan demonstrated a segmental wall thickening of the distal ascending colon with nonspecific multiple small lymphnodes, along the ileocolic vessels, but no signs of mass or obstruction. The histologic findings of resected specimen confirmed EATL type II. Patient expired two weeks after the operation. Therefore, we emphasize the need of random biopsy in the presence of normal mucosa appearance on colonoscopy for the early diagnosis of EATL.
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