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Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature
Esophageal inflammatory myofibroblastic tumors (IMT) are extremely rare, and the understanding on the clinical presentation is limited. IMT of esophagus should be considered as a differential diagnosis in the context of unexplained upper gastrointestinal bleeding and rapidly progressing dysphagia in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771923/ https://www.ncbi.nlm.nih.gov/pubmed/29375843 http://dx.doi.org/10.1002/ccr3.1296 |
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author | Jayarajah, Umesh Bulathsinghala, Rasika P. Handagala, Dassanayake M Sumana Samarasekera, Dharmabandhu Nandadeva |
author_facet | Jayarajah, Umesh Bulathsinghala, Rasika P. Handagala, Dassanayake M Sumana Samarasekera, Dharmabandhu Nandadeva |
author_sort | Jayarajah, Umesh |
collection | PubMed |
description | Esophageal inflammatory myofibroblastic tumors (IMT) are extremely rare, and the understanding on the clinical presentation is limited. IMT of esophagus should be considered as a differential diagnosis in the context of unexplained upper gastrointestinal bleeding and rapidly progressing dysphagia in young patients. |
format | Online Article Text |
id | pubmed-5771923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57719232018-01-26 Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature Jayarajah, Umesh Bulathsinghala, Rasika P. Handagala, Dassanayake M Sumana Samarasekera, Dharmabandhu Nandadeva Clin Case Rep Case Reports Esophageal inflammatory myofibroblastic tumors (IMT) are extremely rare, and the understanding on the clinical presentation is limited. IMT of esophagus should be considered as a differential diagnosis in the context of unexplained upper gastrointestinal bleeding and rapidly progressing dysphagia in young patients. John Wiley and Sons Inc. 2017-11-28 /pmc/articles/PMC5771923/ /pubmed/29375843 http://dx.doi.org/10.1002/ccr3.1296 Text en © 2017 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Jayarajah, Umesh Bulathsinghala, Rasika P. Handagala, Dassanayake M Sumana Samarasekera, Dharmabandhu Nandadeva Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature |
title | Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature |
title_full | Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature |
title_fullStr | Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature |
title_full_unstemmed | Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature |
title_short | Inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature |
title_sort | inflammatory myofibroblastic tumor of the esophagus presenting with hematemesis and melaena: a case report and review of literature |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771923/ https://www.ncbi.nlm.nih.gov/pubmed/29375843 http://dx.doi.org/10.1002/ccr3.1296 |
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