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Updated: Jun 24, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Two challenging cases of anti-MDA-5 dermatomyositis with rapidly progressive interstitial lung disease
Kathryn Biddle1,2, Elif Agaoglu3, Geoffrey Brent4
1St George's University of London, Infection and Immunity, Cranmer Terrace, London, SW17 0RE, UK.
Abstract:
Anti-MDA-5 dermatomyositis (DM) is a subtype of idiopathic inflammatory myopathy, commonly presenting as clinically amyopathic dermatomyositis. It is associated with rapidly progressive interstitial lung disease and a poor prognosis. Here, we present two cases of anti-MDA-5 DM and discuss the challenges associated with timely diagnosis, and the importance of early and aggressive treatment.
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