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IMFT of the sigmoid colon: a case report

Inflammatory myofibroblastic tumor (IMFT) of the colon is a very rare entity, characterized by proliferation of myofibroblast cells admixed with inflammatory infiltrates. The entity was first described in the late 1990s, and since then less than 30 cases have been described. It frequently mimics oth...

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Autores principales: Pandit, Narendra, Yadav, Tek Narayan, Shrestha, Deepa, Adhikari, Purbesh, Awale, Laligen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865348/
https://www.ncbi.nlm.nih.gov/pubmed/31768246
http://dx.doi.org/10.1093/jscr/rjz334
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author Pandit, Narendra
Yadav, Tek Narayan
Shrestha, Deepa
Adhikari, Purbesh
Awale, Laligen
author_facet Pandit, Narendra
Yadav, Tek Narayan
Shrestha, Deepa
Adhikari, Purbesh
Awale, Laligen
author_sort Pandit, Narendra
collection PubMed
description Inflammatory myofibroblastic tumor (IMFT) of the colon is a very rare entity, characterized by proliferation of myofibroblast cells admixed with inflammatory infiltrates. The entity was first described in the late 1990s, and since then less than 30 cases have been described. It frequently mimics other neoplasm of the colon, such as adenocarcinoma, lymphoma and stromal tumor, and is very difficult to clinch the diagnosis preoperatively based on the clinical and radiological findings. Here, we discuss an uncommon case of sigmoid IMFT in a 35-year old male, presenting with bleeding per rectum and managed successfully by colectomy.
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spelling pubmed-68653482019-11-25 IMFT of the sigmoid colon: a case report Pandit, Narendra Yadav, Tek Narayan Shrestha, Deepa Adhikari, Purbesh Awale, Laligen J Surg Case Rep Case Report Inflammatory myofibroblastic tumor (IMFT) of the colon is a very rare entity, characterized by proliferation of myofibroblast cells admixed with inflammatory infiltrates. The entity was first described in the late 1990s, and since then less than 30 cases have been described. It frequently mimics other neoplasm of the colon, such as adenocarcinoma, lymphoma and stromal tumor, and is very difficult to clinch the diagnosis preoperatively based on the clinical and radiological findings. Here, we discuss an uncommon case of sigmoid IMFT in a 35-year old male, presenting with bleeding per rectum and managed successfully by colectomy. Oxford University Press 2019-11-20 /pmc/articles/PMC6865348/ /pubmed/31768246 http://dx.doi.org/10.1093/jscr/rjz334 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2019. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Pandit, Narendra
Yadav, Tek Narayan
Shrestha, Deepa
Adhikari, Purbesh
Awale, Laligen
IMFT of the sigmoid colon: a case report
title IMFT of the sigmoid colon: a case report
title_full IMFT of the sigmoid colon: a case report
title_fullStr IMFT of the sigmoid colon: a case report
title_full_unstemmed IMFT of the sigmoid colon: a case report
title_short IMFT of the sigmoid colon: a case report
title_sort imft of the sigmoid colon: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865348/
https://www.ncbi.nlm.nih.gov/pubmed/31768246
http://dx.doi.org/10.1093/jscr/rjz334
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AT awalelaligen imftofthesigmoidcolonacasereport