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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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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. |
format | Online Article Text |
id | pubmed-5328934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT oliveiracarlos retroperitonealinflammatorymyofibroblastictumoracasereport AT costarui retroperitonealinflammatorymyofibroblastictumoracasereport AT estevaoamelia retroperitonealinflammatorymyofibroblastictumoracasereport AT caseiroalvesfilipe retroperitonealinflammatorymyofibroblastictumoracasereport |