Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/7543
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dc.contributor.authorSleiman, Youssefen_US
dc.contributor.authorHadeer, Ribal Abyen_US
dc.contributor.authorNahle, Hassanen_US
dc.contributor.authorJurdi, Nawafen_US
dc.contributor.authorAbs, Leilaen_US
dc.contributor.authorAllouch, Mustafaen_US
dc.date.accessioned2024-10-03T06:40:02Z-
dc.date.available2024-10-03T06:40:02Z-
dc.date.issued2024-09-21-
dc.identifier.issn2210-2612-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/7543-
dc.description.abstractMonomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) is a very rare and aggressive type of gastrointestinal non-Hodgkin's lymphoma (NHL) with a poor prognosis. Case presentation: A 59-year-old man presented with a three-days history of diffuse abdominal pain associated with distention and obstipation. Abdominal computed tomography (CT) scan showed small bowel obstruction (SBO) due to moderately thickened jejunal loop. The SBO was treated conservatively, and after a workup, the patient underwent a laparoscopic oncological small bowel resection. The final pathology sampling revealed transmural sheets of atypical lymphoid cells that were identified as MEITL, which is a very rare type of small bowel lymphoma, by the histo-immunopathoplogy studies. He responded to three courses of chemotherapy, and the patient went into remission at the end of the third chemotherapy session. Five months post remission patient was rushed to the emergency with acute mesenteric ischemia and died shortly after. Discussion: An extremely uncommon and aggressive type of T-cell lymphoma is called monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL). Gastrointestinal involvement was detected in the majority of the patients. 40 % of the published cases had stage IV disease. Based on morphological classification, the tumors were classified into two groups: Typical (58 %) and atypical (i.e., non-monomorphic or exhibiting necrosis, angiotropism, or starry-sky pattern) (42 %). Mostly caused by driver gene changes that de-regulate JAK/STAT signaling and histone methylation, it is resistant to standard therapy and includes morphologic and genetic variants that carry a very high clinical risk. Conclusion: We report a case of MEITL detected after jejunal resection in a patient presented initially with SBO. Our patient has a recurrence-free survival of 5 months after chemotherapy, but passed away 5 months after remission due to acute mesenteric ischemia.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.subjectCase reporten_US
dc.subjectEnteropathy associated T-cell lymphoma type IIen_US
dc.subjectIntestinal lymphomaen_US
dc.subjectMonomorphic epitheliotrophic intestinal T-cell lymphomaen_US
dc.subjectSmall bowel non Hodgkin lymphomaen_US
dc.subjectSmall bowel obstructionen_US
dc.titleMonomorphic epitheliotropic intestinal T-cell lymphoma with obstructive pattern: A rare case of small bowel lymphomaen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.ijscr.2024.110327-
dc.identifier.pmid39317016-
dc.identifier.scopus2-s2.0-85204424966-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85204424966-
dc.contributor.affiliationFaculty of Medicineen_US
dc.contributor.affiliationFaculty of Medicineen_US
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume124en_US
dc.date.catalogued2024-10-01-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://www.sciencedirect.com/science/article/pii/S2210261224011088en_US
dc.relation.ispartoftextInternational Journal of Surgery Case Reportsen_US
Appears in Collections:Faculty of Medicine
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