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Relapsing Polychondritis

Relapsing polychondritis (RP) is a rare systemic disease characterized by recurrent, widespread chondritis of the auricular, nasal, and tracheal cartilages. Additional clinical features include audiovestibular dysfunction, ocular inflammation, vasculitis, myocarditis, and nonerosive arthritis. Altho...

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Autores principales: Sosada, Beata, Loza, Katarzyna, Bialo-Wojcicka, Ewelina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198788/
https://www.ncbi.nlm.nih.gov/pubmed/25349745
http://dx.doi.org/10.1155/2014/791951
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author Sosada, Beata
Loza, Katarzyna
Bialo-Wojcicka, Ewelina
author_facet Sosada, Beata
Loza, Katarzyna
Bialo-Wojcicka, Ewelina
author_sort Sosada, Beata
collection PubMed
description Relapsing polychondritis (RP) is a rare systemic disease characterized by recurrent, widespread chondritis of the auricular, nasal, and tracheal cartilages. Additional clinical features include audiovestibular dysfunction, ocular inflammation, vasculitis, myocarditis, and nonerosive arthritis. Although the cause remains unknown, the etiology is suspected to be autoimmune. We describe a case of a 31-year-old woman with a four-month history of bilateral auricular and nasal chondritis. Infectious and neoplastic diseases were excluded by imaging and laboratory examinations. RP was diagnosed based on three McAdam's criteria. The patient was medicated with oral prednisolone and methotrexate with positive clinical response. In this case clinical history and detailed physical examination were fundamental in concluding the correct diagnosis and administrating the appropriate medication.
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spelling pubmed-41987882014-10-27 Relapsing Polychondritis Sosada, Beata Loza, Katarzyna Bialo-Wojcicka, Ewelina Case Rep Dermatol Med Case Report Relapsing polychondritis (RP) is a rare systemic disease characterized by recurrent, widespread chondritis of the auricular, nasal, and tracheal cartilages. Additional clinical features include audiovestibular dysfunction, ocular inflammation, vasculitis, myocarditis, and nonerosive arthritis. Although the cause remains unknown, the etiology is suspected to be autoimmune. We describe a case of a 31-year-old woman with a four-month history of bilateral auricular and nasal chondritis. Infectious and neoplastic diseases were excluded by imaging and laboratory examinations. RP was diagnosed based on three McAdam's criteria. The patient was medicated with oral prednisolone and methotrexate with positive clinical response. In this case clinical history and detailed physical examination were fundamental in concluding the correct diagnosis and administrating the appropriate medication. Hindawi Publishing Corporation 2014 2014-09-30 /pmc/articles/PMC4198788/ /pubmed/25349745 http://dx.doi.org/10.1155/2014/791951 Text en Copyright © 2014 Beata Sosada et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sosada, Beata
Loza, Katarzyna
Bialo-Wojcicka, Ewelina
Relapsing Polychondritis
title Relapsing Polychondritis
title_full Relapsing Polychondritis
title_fullStr Relapsing Polychondritis
title_full_unstemmed Relapsing Polychondritis
title_short Relapsing Polychondritis
title_sort relapsing polychondritis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198788/
https://www.ncbi.nlm.nih.gov/pubmed/25349745
http://dx.doi.org/10.1155/2014/791951
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