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Chondromyxoid Fibroma: A Rare Case Report and Review of Literature

Chondromyxoid fibroma (CMF) is one of the rarest benign tumors of cartilaginous origin. It accounts for less than 0.5% of bone tumors and less than two percent of benign bone tumors. It is composed of a mixture of chondroid, myxoid, and fibrous tissues. The diagnosis of CMF depends upon its characte...

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Autores principales: Soni, Rishit, Kapoor, Chirag, Shah, Malkesh, Turakhiya, Jay, Golwala, Paresh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101078/
https://www.ncbi.nlm.nih.gov/pubmed/27833828
http://dx.doi.org/10.7759/cureus.803
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author Soni, Rishit
Kapoor, Chirag
Shah, Malkesh
Turakhiya, Jay
Golwala, Paresh
author_facet Soni, Rishit
Kapoor, Chirag
Shah, Malkesh
Turakhiya, Jay
Golwala, Paresh
author_sort Soni, Rishit
collection PubMed
description Chondromyxoid fibroma (CMF) is one of the rarest benign tumors of cartilaginous origin. It accounts for less than 0.5% of bone tumors and less than two percent of benign bone tumors. It is composed of a mixture of chondroid, myxoid, and fibrous tissues. The diagnosis of CMF depends upon its characteristic histological appearance like a lobular pattern with stellate-shaped cells in a myxoid or chondroid background. We present a case of juxtacortical CMF in a 15-year-old male involving the proximal end of the tibia, which was treated with en bloc excision and bone grafting with excellent results on final follow-up.
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spelling pubmed-51010782016-11-10 Chondromyxoid Fibroma: A Rare Case Report and Review of Literature Soni, Rishit Kapoor, Chirag Shah, Malkesh Turakhiya, Jay Golwala, Paresh Cureus Radiology Chondromyxoid fibroma (CMF) is one of the rarest benign tumors of cartilaginous origin. It accounts for less than 0.5% of bone tumors and less than two percent of benign bone tumors. It is composed of a mixture of chondroid, myxoid, and fibrous tissues. The diagnosis of CMF depends upon its characteristic histological appearance like a lobular pattern with stellate-shaped cells in a myxoid or chondroid background. We present a case of juxtacortical CMF in a 15-year-old male involving the proximal end of the tibia, which was treated with en bloc excision and bone grafting with excellent results on final follow-up. Cureus 2016-09-23 /pmc/articles/PMC5101078/ /pubmed/27833828 http://dx.doi.org/10.7759/cureus.803 Text en Copyright © 2016, Soni et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Radiology
Soni, Rishit
Kapoor, Chirag
Shah, Malkesh
Turakhiya, Jay
Golwala, Paresh
Chondromyxoid Fibroma: A Rare Case Report and Review of Literature
title Chondromyxoid Fibroma: A Rare Case Report and Review of Literature
title_full Chondromyxoid Fibroma: A Rare Case Report and Review of Literature
title_fullStr Chondromyxoid Fibroma: A Rare Case Report and Review of Literature
title_full_unstemmed Chondromyxoid Fibroma: A Rare Case Report and Review of Literature
title_short Chondromyxoid Fibroma: A Rare Case Report and Review of Literature
title_sort chondromyxoid fibroma: a rare case report and review of literature
topic Radiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101078/
https://www.ncbi.nlm.nih.gov/pubmed/27833828
http://dx.doi.org/10.7759/cureus.803
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