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Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma

Inflammatory myofibroblastic tumor (IMT) is a rare, aggressive tumor of indeterminate malignant potential with myofibroblastic differentiation. Though bladder location is very uncommon, it arises from the bladder submucosal stroma as a polypoidal growth and is easily mistaken for a malignant neoplas...

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Autores principales: Singh, Aneeta, Lahori, Mega, Khajuria, Arvind, Gupta, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456893/
https://www.ncbi.nlm.nih.gov/pubmed/26097827
http://dx.doi.org/10.4103/2229-516X.157174
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author Singh, Aneeta
Lahori, Mega
Khajuria, Arvind
Gupta, Sunil
author_facet Singh, Aneeta
Lahori, Mega
Khajuria, Arvind
Gupta, Sunil
author_sort Singh, Aneeta
collection PubMed
description Inflammatory myofibroblastic tumor (IMT) is a rare, aggressive tumor of indeterminate malignant potential with myofibroblastic differentiation. Though bladder location is very uncommon, it arises from the bladder submucosal stroma as a polypoidal growth and is easily mistaken for a malignant neoplasm- clinically, radiologically and histologically. Essential criteria for the diagnosis of IMT are: spindle myoepithelial cell proliferation and lymphoplasmacytic infiltrate. Here we report the case of a 30 years old man who presented with painless gross haematuria for 2 weeks. The patient underwent open partial cystectomy and the final pathological diagnosis was IMT of bladder.
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spelling pubmed-44568932015-06-19 Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma Singh, Aneeta Lahori, Mega Khajuria, Arvind Gupta, Sunil Int J Appl Basic Med Res Case Report Inflammatory myofibroblastic tumor (IMT) is a rare, aggressive tumor of indeterminate malignant potential with myofibroblastic differentiation. Though bladder location is very uncommon, it arises from the bladder submucosal stroma as a polypoidal growth and is easily mistaken for a malignant neoplasm- clinically, radiologically and histologically. Essential criteria for the diagnosis of IMT are: spindle myoepithelial cell proliferation and lymphoplasmacytic infiltrate. Here we report the case of a 30 years old man who presented with painless gross haematuria for 2 weeks. The patient underwent open partial cystectomy and the final pathological diagnosis was IMT of bladder. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4456893/ /pubmed/26097827 http://dx.doi.org/10.4103/2229-516X.157174 Text en Copyright: © International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Singh, Aneeta
Lahori, Mega
Khajuria, Arvind
Gupta, Sunil
Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma
title Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma
title_full Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma
title_fullStr Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma
title_full_unstemmed Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma
title_short Inflammatory myofibroblastic tumor of the urinary bladder: A diagnostic challange and therapeutic dilemma
title_sort inflammatory myofibroblastic tumor of the urinary bladder: a diagnostic challange and therapeutic dilemma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456893/
https://www.ncbi.nlm.nih.gov/pubmed/26097827
http://dx.doi.org/10.4103/2229-516X.157174
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