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Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis
BACKGROUND: Enteropathy associated T-cell lymphoma (EATL) is a rare form of peripheral T-cell lymphoma and makes up less than 5% of gastrointestinal lymphomas. EATL can be divided into type 1 which is associated with celiac disease, and monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL),...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354114/ https://www.ncbi.nlm.nih.gov/pubmed/30705732 http://dx.doi.org/10.4253/wjge.v11.i1.54 |
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author | Fisher, Aaron Yousif, Edward Piper, Marc |
author_facet | Fisher, Aaron Yousif, Edward Piper, Marc |
author_sort | Fisher, Aaron |
collection | PubMed |
description | BACKGROUND: Enteropathy associated T-cell lymphoma (EATL) is a rare form of peripheral T-cell lymphoma and makes up less than 5% of gastrointestinal lymphomas. EATL can be divided into type 1 which is associated with celiac disease, and monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL), formally type 2, which is not associated with celiac disease. CASE SUMMARY: We present a 60-year-old African American female, without celiac disease, who presented with abdominal pain, diarrhea, and 30 lb. weight loss over a 3 month period. She was subsequently diagnosed with EATL throughout her entire gastrointestinal tract. She is currently undergoing chemotherapy with EOCH (Etoposide, Oncovin, Cyclophosphamide, and Hydroxydaunorubicin). EATL is most common in the Asian and Hispanic population yet the incidence in African Americans is uncertain and emphasizes the rarity of this case. A literature review was included to further emphasize similarities and differences between our case and previously reported cases of MEITL. CONCLUSION: The patient was diagnosed with EATL, immunochemical testing was not conclusive for MEITL however was suggestive of the disease. |
format | Online Article Text |
id | pubmed-6354114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-63541142019-01-31 Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis Fisher, Aaron Yousif, Edward Piper, Marc World J Gastrointest Endosc Case Report BACKGROUND: Enteropathy associated T-cell lymphoma (EATL) is a rare form of peripheral T-cell lymphoma and makes up less than 5% of gastrointestinal lymphomas. EATL can be divided into type 1 which is associated with celiac disease, and monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL), formally type 2, which is not associated with celiac disease. CASE SUMMARY: We present a 60-year-old African American female, without celiac disease, who presented with abdominal pain, diarrhea, and 30 lb. weight loss over a 3 month period. She was subsequently diagnosed with EATL throughout her entire gastrointestinal tract. She is currently undergoing chemotherapy with EOCH (Etoposide, Oncovin, Cyclophosphamide, and Hydroxydaunorubicin). EATL is most common in the Asian and Hispanic population yet the incidence in African Americans is uncertain and emphasizes the rarity of this case. A literature review was included to further emphasize similarities and differences between our case and previously reported cases of MEITL. CONCLUSION: The patient was diagnosed with EATL, immunochemical testing was not conclusive for MEITL however was suggestive of the disease. Baishideng Publishing Group Inc 2019-01-16 2019-01-16 /pmc/articles/PMC6354114/ /pubmed/30705732 http://dx.doi.org/10.4253/wjge.v11.i1.54 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Fisher, Aaron Yousif, Edward Piper, Marc Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis |
title | Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis |
title_full | Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis |
title_fullStr | Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis |
title_full_unstemmed | Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis |
title_short | Truth lies below: A case report and literature review of typical appearing polyps yet with an atypical diagnosis |
title_sort | truth lies below: a case report and literature review of typical appearing polyps yet with an atypical diagnosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354114/ https://www.ncbi.nlm.nih.gov/pubmed/30705732 http://dx.doi.org/10.4253/wjge.v11.i1.54 |
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