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An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease

Some cases of psoriatic arthritis (PsA) cannot be explicitly diagnosed, especially when the skin and nail lesions present years after the joint disease or are absent. Autoimmunity may also play a role in the development of Dupuytren's disease. However, the simultaneous presence of PsA and Dupuy...

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Autores principales: Ding, Wen Quan, Gu, Jian Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publicaitons 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386194/
https://www.ncbi.nlm.nih.gov/pubmed/25878651
http://dx.doi.org/10.12669/pjms.311.6079
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author Ding, Wen Quan
Gu, Jian Hui
author_facet Ding, Wen Quan
Gu, Jian Hui
author_sort Ding, Wen Quan
collection PubMed
description Some cases of psoriatic arthritis (PsA) cannot be explicitly diagnosed, especially when the skin and nail lesions present years after the joint disease or are absent. Autoimmunity may also play a role in the development of Dupuytren's disease. However, the simultaneous presence of PsA and Dupuytren’s disease is very rare. We present a patient displaying arthritis in multiple small joints, with bone erosions and bony fusions in all four extremities, combined with Dupuytren’s disease. Because of the atypical clinical manifestation, the diagnosis perplexed doctors for decades. Without formal treatment, the disease followed a natural course over time. Reviewing the patient’s data, a potential diagnosis of PsA, combined with Dupuytren’s disease, was eventually made. After surgery, contractures of palmar and plantar fascia as well the thumb web were released, and the hallux valgus was corrected.
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spelling pubmed-43861942015-04-15 An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease Ding, Wen Quan Gu, Jian Hui Pak J Med Sci Case Report Some cases of psoriatic arthritis (PsA) cannot be explicitly diagnosed, especially when the skin and nail lesions present years after the joint disease or are absent. Autoimmunity may also play a role in the development of Dupuytren's disease. However, the simultaneous presence of PsA and Dupuytren’s disease is very rare. We present a patient displaying arthritis in multiple small joints, with bone erosions and bony fusions in all four extremities, combined with Dupuytren’s disease. Because of the atypical clinical manifestation, the diagnosis perplexed doctors for decades. Without formal treatment, the disease followed a natural course over time. Reviewing the patient’s data, a potential diagnosis of PsA, combined with Dupuytren’s disease, was eventually made. After surgery, contractures of palmar and plantar fascia as well the thumb web were released, and the hallux valgus was corrected. Professional Medical Publicaitons 2015 /pmc/articles/PMC4386194/ /pubmed/25878651 http://dx.doi.org/10.12669/pjms.311.6079 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ding, Wen Quan
Gu, Jian Hui
An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease
title An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease
title_full An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease
title_fullStr An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease
title_full_unstemmed An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease
title_short An intractable case of suspected psoriatic arthritis combined with Dupuytren’s disease
title_sort intractable case of suspected psoriatic arthritis combined with dupuytren’s disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386194/
https://www.ncbi.nlm.nih.gov/pubmed/25878651
http://dx.doi.org/10.12669/pjms.311.6079
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