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Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review

Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare low-grade, malignant soft tissue tumor that is usually observed in the extremities of adult patients. Magnetic resonance imaging findings for this tumor type have rarely been reported. We report a case involving the distal left femur of a middle...

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Autores principales: Togral, Guray, Arikan, Murat, Aktas, Elif, Gungor, Safak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135371/
https://www.ncbi.nlm.nih.gov/pubmed/25011461
http://dx.doi.org/10.5732/cjc.014.10049
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author Togral, Guray
Arikan, Murat
Aktas, Elif
Gungor, Safak
author_facet Togral, Guray
Arikan, Murat
Aktas, Elif
Gungor, Safak
author_sort Togral, Guray
collection PubMed
description Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare low-grade, malignant soft tissue tumor that is usually observed in the extremities of adult patients. Magnetic resonance imaging findings for this tumor type have rarely been reported. We report a case involving the distal left femur of a middle-aged man and tumoral invasion of the bone, which, to our knowledge, has been previously described only once. He was treated with distal femoral tumor resection and reconstruction with a modular prosthesis. Histopathologic diagnosis confirmed MIFS. We reviewed literature of the diagnostic imaging and bone invasion findings associated with this tumor type.
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spelling pubmed-41353712014-08-28 Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review Togral, Guray Arikan, Murat Aktas, Elif Gungor, Safak Chin J Cancer Case Research Myxoinflammatory fibroblastic sarcoma (MIFS) is a rare low-grade, malignant soft tissue tumor that is usually observed in the extremities of adult patients. Magnetic resonance imaging findings for this tumor type have rarely been reported. We report a case involving the distal left femur of a middle-aged man and tumoral invasion of the bone, which, to our knowledge, has been previously described only once. He was treated with distal femoral tumor resection and reconstruction with a modular prosthesis. Histopathologic diagnosis confirmed MIFS. We reviewed literature of the diagnostic imaging and bone invasion findings associated with this tumor type. Sun Yat-sen University Cancer Center 2014-08 /pmc/articles/PMC4135371/ /pubmed/25011461 http://dx.doi.org/10.5732/cjc.014.10049 Text en Chinese Journal of Cancer 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-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Case Research
Togral, Guray
Arikan, Murat
Aktas, Elif
Gungor, Safak
Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review
title Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review
title_full Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review
title_fullStr Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review
title_full_unstemmed Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review
title_short Giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review
title_sort giant myxoinflammatory fibroblastic sarcoma with bone invasion: a very rare clinical entity and literature review
topic Case Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135371/
https://www.ncbi.nlm.nih.gov/pubmed/25011461
http://dx.doi.org/10.5732/cjc.014.10049
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