Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case

Primary inflammatory myofibroblastic tumor (IMT) is a very rare tumor arising from stomach and it closely mimics gastric GIST. It usually affects the lung and found in children and young patients. The diagnosis of gastric IMT is usually done post-operatively by immunohistochemistry examination where...

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Autores principales: Hajong, Ranendra, Newme, Kewithinwangbo, Khongwar, Donkupar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132761/
https://www.ncbi.nlm.nih.gov/pubmed/34017787
http://dx.doi.org/10.4103/jfmpc.jfmpc_1126_20
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author Hajong, Ranendra
Newme, Kewithinwangbo
Khongwar, Donkupar
author_facet Hajong, Ranendra
Newme, Kewithinwangbo
Khongwar, Donkupar
author_sort Hajong, Ranendra
collection PubMed
description Primary inflammatory myofibroblastic tumor (IMT) is a very rare tumor arising from stomach and it closely mimics gastric GIST. It usually affects the lung and found in children and young patients. The diagnosis of gastric IMT is usually done post-operatively by immunohistochemistry examination where it is seen that IMT is positive to SMA and vimentin. Complete surgical excision is the treatment of choice and local recurrence is usually seen in incompletely resected cases.
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spelling pubmed-81327612021-05-19 Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case Hajong, Ranendra Newme, Kewithinwangbo Khongwar, Donkupar J Family Med Prim Care Case Report Primary inflammatory myofibroblastic tumor (IMT) is a very rare tumor arising from stomach and it closely mimics gastric GIST. It usually affects the lung and found in children and young patients. The diagnosis of gastric IMT is usually done post-operatively by immunohistochemistry examination where it is seen that IMT is positive to SMA and vimentin. Complete surgical excision is the treatment of choice and local recurrence is usually seen in incompletely resected cases. Wolters Kluwer - Medknow 2021-01 2021-01-30 /pmc/articles/PMC8132761/ /pubmed/34017787 http://dx.doi.org/10.4103/jfmpc.jfmpc_1126_20 Text en Copyright: © 2021 Journal of Family Medicine and Primary Care https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Hajong, Ranendra
Newme, Kewithinwangbo
Khongwar, Donkupar
Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case
title Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case
title_full Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case
title_fullStr Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case
title_full_unstemmed Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case
title_short Primary inflammatory myofibroblastic tumor of stomach—report of a very rare case
title_sort primary inflammatory myofibroblastic tumor of stomach—report of a very rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132761/
https://www.ncbi.nlm.nih.gov/pubmed/34017787
http://dx.doi.org/10.4103/jfmpc.jfmpc_1126_20
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