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A Case of Lung Involvement Associated with Juvenile Idiopathic Arthritis
Author(s) -
Chung Mo Koo,
Seong Yeol Choi,
Jong Gyun Ahn,
Ki Hwan Kim,
Dong Soo Kim
Publication year - 2013
Publication title -
journal of rheumatic diseases
Language(s) - English
Resource type - Journals
eISSN - 2093-940X
pISSN - 2233-4718
DOI - 10.4078/jrd.2013.20.5.332
Subject(s) - juvenile , arthritis , medicine , lung , biology , genetics
Juvenile idiopathic arthritis (JIA) can develop extra-articular manifestations, including growth retardation, osteopenia and chronic uveitis. However, pleuropulmonary involvement is rare. Approximately 40% of patients with JIA have abnormal pulmonary function tests without pulmonary symptoms, with the commonest abnormality in carbon monoxide diffusing capacity, but clinically evident pulmonary parenchymal disease in JIA is extremely uncommon. We describe a 15-year-old male with JIA who presented with dyspnea due to interstitial lung disease.

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