Abstract
Juvenile idiopathic arthritis (JIA) can develop extraarticular 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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Figure 1.
Chest PA shows pneumomediastinum (white arrow head), right pleural effusion (black arrow) and honeycombing in Left Lower lobe (white arrow).
![jrd-20-332f1.tif](/upload/SynapseXML/1010jrd/thumb/jrd-20-332f1.gif)