Monomorphic epitheliotropic intestinal T-cell lymphomas: a case report

Abstract Background Monomorphic epitheliotropic intestinal T-cell lymphomas (MEITL) is a rare and aggressive subtype of lymphoma. The most common site of origin is small intestine. Patients are often presented with diagnosis of intestinal perforation with abdominal pain as the main consulting sympto...

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Main Authors: Haibin Zhong, Yang Zheng, Feiran Zhang
Format: Article
Language:English
Published: BMC 2021-08-01
Series:Diagnostic Pathology
Subjects:
Online Access:https://doi.org/10.1186/s13000-021-01143-x
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author Haibin Zhong
Yang Zheng
Feiran Zhang
author_facet Haibin Zhong
Yang Zheng
Feiran Zhang
author_sort Haibin Zhong
collection DOAJ
description Abstract Background Monomorphic epitheliotropic intestinal T-cell lymphomas (MEITL) is a rare and aggressive subtype of lymphoma. The most common site of origin is small intestine. Patients are often presented with diagnosis of intestinal perforation with abdominal pain as the main consulting symptoms. Because of the deficiency of specific diagnostic measures and effective management, diagnosis is often confirmed in advanced stage with poor prognosis. Case presentation Here, we introduce a patient who has suffered from abdominal pain and diarrhea, and eventually been diagnosed as Monomorphic epitheliotropic intestinal T-cell lymphomas. Conclusion MEITL is rare in clinical practice with deficiency of early diagnostic measures and poor prognosis. Therefore, any patient with ambiguous gastrointestinal symptoms or perforation of the digestive tract where the primary lesion is difficult to identify should be alert to the possibility of this disease.
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spelling doaj.art-8d28fc781862476f8e2bfa597eddeb0a2022-12-21T22:38:05ZengBMCDiagnostic Pathology1746-15962021-08-011611510.1186/s13000-021-01143-xMonomorphic epitheliotropic intestinal T-cell lymphomas: a case reportHaibin Zhong0Yang Zheng1Feiran Zhang2Department of General Surgery, The First Affiliated Hospital of Shantou University Medical CollegeDepartment of General Surgery, The First Affiliated Hospital of Shantou University Medical CollegeDepartment of General Surgery, The First Affiliated Hospital of Shantou University Medical CollegeAbstract Background Monomorphic epitheliotropic intestinal T-cell lymphomas (MEITL) is a rare and aggressive subtype of lymphoma. The most common site of origin is small intestine. Patients are often presented with diagnosis of intestinal perforation with abdominal pain as the main consulting symptoms. Because of the deficiency of specific diagnostic measures and effective management, diagnosis is often confirmed in advanced stage with poor prognosis. Case presentation Here, we introduce a patient who has suffered from abdominal pain and diarrhea, and eventually been diagnosed as Monomorphic epitheliotropic intestinal T-cell lymphomas. Conclusion MEITL is rare in clinical practice with deficiency of early diagnostic measures and poor prognosis. Therefore, any patient with ambiguous gastrointestinal symptoms or perforation of the digestive tract where the primary lesion is difficult to identify should be alert to the possibility of this disease.https://doi.org/10.1186/s13000-021-01143-xMonomorphic epitheliotropic intestinal T-cell lymphomasDiagnosisPrognosisCase report
spellingShingle Haibin Zhong
Yang Zheng
Feiran Zhang
Monomorphic epitheliotropic intestinal T-cell lymphomas: a case report
Diagnostic Pathology
Monomorphic epitheliotropic intestinal T-cell lymphomas
Diagnosis
Prognosis
Case report
title Monomorphic epitheliotropic intestinal T-cell lymphomas: a case report
title_full Monomorphic epitheliotropic intestinal T-cell lymphomas: a case report
title_fullStr Monomorphic epitheliotropic intestinal T-cell lymphomas: a case report
title_full_unstemmed Monomorphic epitheliotropic intestinal T-cell lymphomas: a case report
title_short Monomorphic epitheliotropic intestinal T-cell lymphomas: a case report
title_sort monomorphic epitheliotropic intestinal t cell lymphomas a case report
topic Monomorphic epitheliotropic intestinal T-cell lymphomas
Diagnosis
Prognosis
Case report
url https://doi.org/10.1186/s13000-021-01143-x
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AT yangzheng monomorphicepitheliotropicintestinaltcelllymphomasacasereport
AT feiranzhang monomorphicepitheliotropicintestinaltcelllymphomasacasereport