Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review

Chondromyxoid fibroma (CMF) is a rare benign bone tumor of cartilaginous origin, with an extremely rare craniofacial occurrence. Considering its rarity, craniofacial CMF presents a diagnostic challenge for radiologists. To our knowledge, only seven cases of zygomatic CMF have been described in the l...

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Autores principales: Zeinoddini, Atefeh, Bezold, Amy, Ezzeldin, Obadah, AL Jadiry, Huda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Institute of Radiology. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749392/
https://www.ncbi.nlm.nih.gov/pubmed/35047203
http://dx.doi.org/10.1259/bjrcr.20210008
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author Zeinoddini, Atefeh
Bezold, Amy
Ezzeldin, Obadah
AL Jadiry, Huda
author_facet Zeinoddini, Atefeh
Bezold, Amy
Ezzeldin, Obadah
AL Jadiry, Huda
author_sort Zeinoddini, Atefeh
collection PubMed
description Chondromyxoid fibroma (CMF) is a rare benign bone tumor of cartilaginous origin, with an extremely rare craniofacial occurrence. Considering its rarity, craniofacial CMF presents a diagnostic challenge for radiologists. To our knowledge, only seven cases of zygomatic CMF have been described in the literature, only one of which was in the paediatric age group. Furthermore, none of the currently reported cases include MRI findings of zygomatic CMF. Here, we present a paediatric case of CMF of the zygoma with a comprehensive literature review of the reported cases, focusing on their radiological features and its differential diagnosis.
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spelling pubmed-87493922022-01-18 Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review Zeinoddini, Atefeh Bezold, Amy Ezzeldin, Obadah AL Jadiry, Huda BJR Case Rep Case Report Chondromyxoid fibroma (CMF) is a rare benign bone tumor of cartilaginous origin, with an extremely rare craniofacial occurrence. Considering its rarity, craniofacial CMF presents a diagnostic challenge for radiologists. To our knowledge, only seven cases of zygomatic CMF have been described in the literature, only one of which was in the paediatric age group. Furthermore, none of the currently reported cases include MRI findings of zygomatic CMF. Here, we present a paediatric case of CMF of the zygoma with a comprehensive literature review of the reported cases, focusing on their radiological features and its differential diagnosis. The British Institute of Radiology. 2021-05-12 /pmc/articles/PMC8749392/ /pubmed/35047203 http://dx.doi.org/10.1259/bjrcr.20210008 Text en © 2021 The Authors. Published by the British Institute of Radiology https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Zeinoddini, Atefeh
Bezold, Amy
Ezzeldin, Obadah
AL Jadiry, Huda
Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review
title Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review
title_full Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review
title_fullStr Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review
title_full_unstemmed Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review
title_short Radiological manifestations of chondromyxoid fibroma in the zygoma: A case report and literature review
title_sort radiological manifestations of chondromyxoid fibroma in the zygoma: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749392/
https://www.ncbi.nlm.nih.gov/pubmed/35047203
http://dx.doi.org/10.1259/bjrcr.20210008
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