Year 2024 / Volume 116 / Number 10
Letter
Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) complicated with intestinal obstruction and perforation

569-571

DOI: 10.17235/reed.2024.10407/2024

Macarena Soto Dopazo, Yaiza Rey Fanjul, Pablo Chamorro Chamorro, María Desirée Díaz González,

Abstract
We report the case of a patient who comes to the emergency department with abdominal pain, oral intolerance and bloody stools, being diagnosed with intestinal obstruction secondary to a jejunal tumor with contained perforation. A laparotomy was performed with resection of the jejunal tumor and taking biopsies from lesions with similar characteristics in the rest of the small bowel compatible with monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL). The monomorphic epitheliotropic intestinal T-cell lymphoma is a rare intestinal tumor with a poor prognosis that is characterized by the proliferation of intraepithelial lymphocytes. The abdominal symptoms are nonspecific and the known major complications are intestinal perforation and obstruction. There is no standard therapeutic approach, being a combination of surgical resection, chemotherapy and autologous stem cell transplant.
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References
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Soto Dopazo M, Rey Fanjul Y, Chamorro Chamorro P, Díaz González M. Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) complicated with intestinal obstruction and perforation. 10407/2024


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Publication history

Received: 16/03/2024

Accepted: 06/04/2024

Online First: 20/05/2024

Published: 09/10/2024

Article Online First time: 65 days

Article editing time: 207 days


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