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Systemic juvenile idiopathic arthritis as a fever of unknown origin

Juvenile idiopathic arthritis (JIA) is a rare inflammation with still unidentified cause. It can also be cause of fever of unknown origin. Diagnosis is made by eliminating infection, malignancy, and rheumatological diseases. In this report, case of a 5-year-old patient with symptoms of intermittent...

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Detalles Bibliográficos
Autores principales: Hardal, Cigdem, Erguven, Muferet, Saglam, Zuhal Aydan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530164/
https://www.ncbi.nlm.nih.gov/pubmed/28752149
http://dx.doi.org/10.14744/nci.2016.07769
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author Hardal, Cigdem
Erguven, Muferet
Saglam, Zuhal Aydan
author_facet Hardal, Cigdem
Erguven, Muferet
Saglam, Zuhal Aydan
author_sort Hardal, Cigdem
collection PubMed
description Juvenile idiopathic arthritis (JIA) is a rare inflammation with still unidentified cause. It can also be cause of fever of unknown origin. Diagnosis is made by eliminating infection, malignancy, and rheumatological diseases. In this report, case of a 5-year-old patient with symptoms of intermittent fever, areas of rash on the body, itching, and swelling, redness, and pain in the right and left ankle is described. Serological test results were negative for infectious agents, and malignancy was excluded. Patient was diagnosed with systemic JIA associated with intermittent fever, negative rheumatological markers and negative serology test results. Treatment with methylprednisolone and methotrexate yielded positive clinical response. Diagnosis of systemic JIA can be challenging, and must be made by eliminating other diseases.
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spelling pubmed-55301642017-07-27 Systemic juvenile idiopathic arthritis as a fever of unknown origin Hardal, Cigdem Erguven, Muferet Saglam, Zuhal Aydan North Clin Istanb Case Report Juvenile idiopathic arthritis (JIA) is a rare inflammation with still unidentified cause. It can also be cause of fever of unknown origin. Diagnosis is made by eliminating infection, malignancy, and rheumatological diseases. In this report, case of a 5-year-old patient with symptoms of intermittent fever, areas of rash on the body, itching, and swelling, redness, and pain in the right and left ankle is described. Serological test results were negative for infectious agents, and malignancy was excluded. Patient was diagnosed with systemic JIA associated with intermittent fever, negative rheumatological markers and negative serology test results. Treatment with methylprednisolone and methotrexate yielded positive clinical response. Diagnosis of systemic JIA can be challenging, and must be made by eliminating other diseases. Kare Publishing 2017-05-10 /pmc/articles/PMC5530164/ /pubmed/28752149 http://dx.doi.org/10.14744/nci.2016.07769 Text en Copyright: © 2017 by Istanbul Northern Anatolian Association of Public Hospitals http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Case Report
Hardal, Cigdem
Erguven, Muferet
Saglam, Zuhal Aydan
Systemic juvenile idiopathic arthritis as a fever of unknown origin
title Systemic juvenile idiopathic arthritis as a fever of unknown origin
title_full Systemic juvenile idiopathic arthritis as a fever of unknown origin
title_fullStr Systemic juvenile idiopathic arthritis as a fever of unknown origin
title_full_unstemmed Systemic juvenile idiopathic arthritis as a fever of unknown origin
title_short Systemic juvenile idiopathic arthritis as a fever of unknown origin
title_sort systemic juvenile idiopathic arthritis as a fever of unknown origin
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530164/
https://www.ncbi.nlm.nih.gov/pubmed/28752149
http://dx.doi.org/10.14744/nci.2016.07769
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