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Fibrocartilaginous dysplasia: What do we know so far?

Fibrocartilaginous dysplasia has been described as a rare variant of fibrous dysplasia. This lesion will appear in imaging as ground glass matrix similar to fibrous dysplasia, but it will also show rings and arcs calcifications. In turn, this can lead to misdiagnosing fibrocartilaginous dysplasia as...

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Autores principales: Alshalan, Asma, Asiri, Yasser, AlGarni, Ayed, Tayara, Bader
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011050/
https://www.ncbi.nlm.nih.gov/pubmed/36926535
http://dx.doi.org/10.1016/j.radcr.2023.01.074
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author Alshalan, Asma
Asiri, Yasser
AlGarni, Ayed
Tayara, Bader
author_facet Alshalan, Asma
Asiri, Yasser
AlGarni, Ayed
Tayara, Bader
author_sort Alshalan, Asma
collection PubMed
description Fibrocartilaginous dysplasia has been described as a rare variant of fibrous dysplasia. This lesion will appear in imaging as ground glass matrix similar to fibrous dysplasia, but it will also show rings and arcs calcifications. In turn, this can lead to misdiagnosing fibrocartilaginous dysplasia as primary cartilaginous lesion such as enchondroma or chondrosarcoma, neccesating histopathological confirmation. We report a case of fibrocartilaginous dysplasia in a 19 years old male with polyostotic fibrous dysplasia with prior pathologic fracture of the left femur. The patient presented with progressive swelling of the left thigh, imaging was done and showed enlargement of the fibrous dysplasia in the left femur with new rings and arcs matrix mineralization. The lesion was biopsied and microscopic evaluation revealed mainly cartilage islands with fibro-osseous tissue. We also discuss the possible origin of the cartilaginous component in this lesion, and its clinical course.
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spelling pubmed-100110502023-03-15 Fibrocartilaginous dysplasia: What do we know so far? Alshalan, Asma Asiri, Yasser AlGarni, Ayed Tayara, Bader Radiol Case Rep Case Report Fibrocartilaginous dysplasia has been described as a rare variant of fibrous dysplasia. This lesion will appear in imaging as ground glass matrix similar to fibrous dysplasia, but it will also show rings and arcs calcifications. In turn, this can lead to misdiagnosing fibrocartilaginous dysplasia as primary cartilaginous lesion such as enchondroma or chondrosarcoma, neccesating histopathological confirmation. We report a case of fibrocartilaginous dysplasia in a 19 years old male with polyostotic fibrous dysplasia with prior pathologic fracture of the left femur. The patient presented with progressive swelling of the left thigh, imaging was done and showed enlargement of the fibrous dysplasia in the left femur with new rings and arcs matrix mineralization. The lesion was biopsied and microscopic evaluation revealed mainly cartilage islands with fibro-osseous tissue. We also discuss the possible origin of the cartilaginous component in this lesion, and its clinical course. Elsevier 2023-02-28 /pmc/articles/PMC10011050/ /pubmed/36926535 http://dx.doi.org/10.1016/j.radcr.2023.01.074 Text en © 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://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 Case Report
Alshalan, Asma
Asiri, Yasser
AlGarni, Ayed
Tayara, Bader
Fibrocartilaginous dysplasia: What do we know so far?
title Fibrocartilaginous dysplasia: What do we know so far?
title_full Fibrocartilaginous dysplasia: What do we know so far?
title_fullStr Fibrocartilaginous dysplasia: What do we know so far?
title_full_unstemmed Fibrocartilaginous dysplasia: What do we know so far?
title_short Fibrocartilaginous dysplasia: What do we know so far?
title_sort fibrocartilaginous dysplasia: what do we know so far?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011050/
https://www.ncbi.nlm.nih.gov/pubmed/36926535
http://dx.doi.org/10.1016/j.radcr.2023.01.074
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