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Early stage fibrodysplasia ossificans progressiva: A case report

Fibrodysplasia ossificans progressiva is a very rare autosomal dominant genetic connective tissue disease with a progressive ectopic ossification of muscle (intramuscular) or perimuscular connective tissue such as tendons or joint capsules. The osseous masses produced will form bridges that abnormal...

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Detalles Bibliográficos
Autores principales: Kamal, Achmad Fauzi, Aprilya, Dina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921199/
https://www.ncbi.nlm.nih.gov/pubmed/31885762
http://dx.doi.org/10.1016/j.radcr.2019.11.009
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author Kamal, Achmad Fauzi
Aprilya, Dina
author_facet Kamal, Achmad Fauzi
Aprilya, Dina
author_sort Kamal, Achmad Fauzi
collection PubMed
description Fibrodysplasia ossificans progressiva is a very rare autosomal dominant genetic connective tissue disease with a progressive ectopic ossification of muscle (intramuscular) or perimuscular connective tissue such as tendons or joint capsules. The osseous masses produced will form bridges that abnormally connect sections of the skeleton, causing disfiguration and normal motor function inhibition. We reported a 5-year-old girl with multiple hard nodules on the back region which initially present as a painful soft mass on the posterior neck region. As the pain subsided, the mass hardened and also appeared in other parts of her back. We decided not to do a biopsy or excisional surgery to prevent flaring up of the disease. Early diagnosis prevents catastrophic diagnostic and treatment procedures. The progressive nature of this disease is difficult to stop but we should delay it as much as possible by preventing muscle trauma, giving disease modifying agent and long-term physiotherapy to counter further disabilities which will eventually develop.
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spelling pubmed-69211992019-12-27 Early stage fibrodysplasia ossificans progressiva: A case report Kamal, Achmad Fauzi Aprilya, Dina Radiol Case Rep Musculoskeletal Fibrodysplasia ossificans progressiva is a very rare autosomal dominant genetic connective tissue disease with a progressive ectopic ossification of muscle (intramuscular) or perimuscular connective tissue such as tendons or joint capsules. The osseous masses produced will form bridges that abnormally connect sections of the skeleton, causing disfiguration and normal motor function inhibition. We reported a 5-year-old girl with multiple hard nodules on the back region which initially present as a painful soft mass on the posterior neck region. As the pain subsided, the mass hardened and also appeared in other parts of her back. We decided not to do a biopsy or excisional surgery to prevent flaring up of the disease. Early diagnosis prevents catastrophic diagnostic and treatment procedures. The progressive nature of this disease is difficult to stop but we should delay it as much as possible by preventing muscle trauma, giving disease modifying agent and long-term physiotherapy to counter further disabilities which will eventually develop. Elsevier 2019-12-13 /pmc/articles/PMC6921199/ /pubmed/31885762 http://dx.doi.org/10.1016/j.radcr.2019.11.009 Text en © 2019 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://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 Musculoskeletal
Kamal, Achmad Fauzi
Aprilya, Dina
Early stage fibrodysplasia ossificans progressiva: A case report
title Early stage fibrodysplasia ossificans progressiva: A case report
title_full Early stage fibrodysplasia ossificans progressiva: A case report
title_fullStr Early stage fibrodysplasia ossificans progressiva: A case report
title_full_unstemmed Early stage fibrodysplasia ossificans progressiva: A case report
title_short Early stage fibrodysplasia ossificans progressiva: A case report
title_sort early stage fibrodysplasia ossificans progressiva: a case report
topic Musculoskeletal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921199/
https://www.ncbi.nlm.nih.gov/pubmed/31885762
http://dx.doi.org/10.1016/j.radcr.2019.11.009
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