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Retroperitoneal inflammatory myofibroblastic tumor: A case report

Inflammatory myofibroblastic tumors (IMT) were previously included in the “inflammatory pseudotumors” family, but have emerged as a distinct entity recently. The management of IMT may be challenging due to its intermediate malignant potential. We present a case of a young patient with an asymptomati...

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Detalles Bibliográficos
Autores principales: Oliveira, Carlos, Costa, Rui, Estêvão, Amélia, Caseiro-Alves, Filipe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328934/
https://www.ncbi.nlm.nih.gov/pubmed/28275656
http://dx.doi.org/10.1016/j.ejro.2017.01.003
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author Oliveira, Carlos
Costa, Rui
Estêvão, Amélia
Caseiro-Alves, Filipe
author_facet Oliveira, Carlos
Costa, Rui
Estêvão, Amélia
Caseiro-Alves, Filipe
author_sort Oliveira, Carlos
collection PubMed
description Inflammatory myofibroblastic tumors (IMT) were previously included in the “inflammatory pseudotumors” family, but have emerged as a distinct entity recently. The management of IMT may be challenging due to its intermediate malignant potential. We present a case of a young patient with an asymptomatic retroperitoneal mass with some imaging findings that could point to the IMT diagnosis pre-operatively. After two failed attempts to fully characterize the lesion by percutaneous and surgical biopsy, surgical resection was conducted and the final diagnosis was achieved.
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spelling pubmed-53289342017-03-08 Retroperitoneal inflammatory myofibroblastic tumor: A case report Oliveira, Carlos Costa, Rui Estêvão, Amélia Caseiro-Alves, Filipe Eur J Radiol Open Article Inflammatory myofibroblastic tumors (IMT) were previously included in the “inflammatory pseudotumors” family, but have emerged as a distinct entity recently. The management of IMT may be challenging due to its intermediate malignant potential. We present a case of a young patient with an asymptomatic retroperitoneal mass with some imaging findings that could point to the IMT diagnosis pre-operatively. After two failed attempts to fully characterize the lesion by percutaneous and surgical biopsy, surgical resection was conducted and the final diagnosis was achieved. Elsevier 2017-02-27 /pmc/articles/PMC5328934/ /pubmed/28275656 http://dx.doi.org/10.1016/j.ejro.2017.01.003 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Oliveira, Carlos
Costa, Rui
Estêvão, Amélia
Caseiro-Alves, Filipe
Retroperitoneal inflammatory myofibroblastic tumor: A case report
title Retroperitoneal inflammatory myofibroblastic tumor: A case report
title_full Retroperitoneal inflammatory myofibroblastic tumor: A case report
title_fullStr Retroperitoneal inflammatory myofibroblastic tumor: A case report
title_full_unstemmed Retroperitoneal inflammatory myofibroblastic tumor: A case report
title_short Retroperitoneal inflammatory myofibroblastic tumor: A case report
title_sort retroperitoneal inflammatory myofibroblastic tumor: a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328934/
https://www.ncbi.nlm.nih.gov/pubmed/28275656
http://dx.doi.org/10.1016/j.ejro.2017.01.003
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