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Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy

Inflammatory myofibroblastic tumor (IMFT) or pseudotumor is a rare tumor that can be seen in various organs. It is an enigmatic tumor of unknown etiology and difficult to differentiate from malignancy, clinically as well as radiologically. Histologically, it is composed of variable proportions of pr...

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Autores principales: Navale, Pooja, Menon, Santosh, Bakshi, Ganesh, Pruthy, Ritesh, Desai, Sangeeta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932604/
https://www.ncbi.nlm.nih.gov/pubmed/24604966
http://dx.doi.org/10.4103/0971-5851.125257
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author Navale, Pooja
Menon, Santosh
Bakshi, Ganesh
Pruthy, Ritesh
Desai, Sangeeta
author_facet Navale, Pooja
Menon, Santosh
Bakshi, Ganesh
Pruthy, Ritesh
Desai, Sangeeta
author_sort Navale, Pooja
collection PubMed
description Inflammatory myofibroblastic tumor (IMFT) or pseudotumor is a rare tumor that can be seen in various organs. It is an enigmatic tumor of unknown etiology and difficult to differentiate from malignancy, clinically as well as radiologically. Histologically, it is composed of variable proportions of proliferating spindle myofibroblasts, fibroblasts, extracellular collagen, lymphocytes and plasma cells. This mainly affects the urinary bladder or prostate. Renal involvement is extremely rare and may pose diagnostic difficulty to the clinician. We describe a renal IMFT, mimicking renal malignancy, having unusual histological features.
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spelling pubmed-39326042014-03-06 Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy Navale, Pooja Menon, Santosh Bakshi, Ganesh Pruthy, Ritesh Desai, Sangeeta Indian J Med Paediatr Oncol Case Report Inflammatory myofibroblastic tumor (IMFT) or pseudotumor is a rare tumor that can be seen in various organs. It is an enigmatic tumor of unknown etiology and difficult to differentiate from malignancy, clinically as well as radiologically. Histologically, it is composed of variable proportions of proliferating spindle myofibroblasts, fibroblasts, extracellular collagen, lymphocytes and plasma cells. This mainly affects the urinary bladder or prostate. Renal involvement is extremely rare and may pose diagnostic difficulty to the clinician. We describe a renal IMFT, mimicking renal malignancy, having unusual histological features. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3932604/ /pubmed/24604966 http://dx.doi.org/10.4103/0971-5851.125257 Text en Copyright: © Indian Journal of Medical and Paediatric Oncology 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
Navale, Pooja
Menon, Santosh
Bakshi, Ganesh
Pruthy, Ritesh
Desai, Sangeeta
Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy
title Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy
title_full Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy
title_fullStr Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy
title_full_unstemmed Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy
title_short Inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: An unusual case mimicking a renal malignancy
title_sort inflammatory myofibroblastic tumor of kidney with heterotopic bone formation: an unusual case mimicking a renal malignancy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932604/
https://www.ncbi.nlm.nih.gov/pubmed/24604966
http://dx.doi.org/10.4103/0971-5851.125257
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