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Advisor(s)
Abstract(s)
The authors report a clinical case of a woman who had a 3 years diagnosis of hipersensitivity pneumonitis based on intersticial lung disease whithout other manifestations. The diagnosis of antisynthetase syndrome was made three years after the initial symptoms upon the onset of systemic manifestations with articular involvement, myositis and determination of anti-PL 7 antibodies. In this syndrome, the isolated pulmonary involvement is rare.
Description
Keywords
Doença Pulmonar Intersticial
Citation
Acta Reumatol Port. 2009 Apr-Jun;34(2):256-60
Publisher
Sociedade Portuguesa de Reumatologia