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Dermatomyositis (DM), which predominantly affects the skin and muscles, is a prevalent subtype within the IIM spectrum. Interstitial lung disease (ILD) is a common comorbidity in DM, with an incidence varying widely from 5% to 65% [1]. The clinical presentations, treatment responses, and outcomes of IIMs are highly variable and correlate with the presence of specific myositis-specific antibodies (MSAs).
J Med Internet Res 2025;27:e62836
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