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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2017
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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. |
format | Online Article Text |
id | pubmed-5530164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
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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