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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2016
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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. |
format | Online Article Text |
id | pubmed-5101078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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