Clinically amyopathic dermatomyositis (CADM), a rare idiopathic inflammatory disease with an estimated incidence of 2 per 1 million people is often concomitantly associated with rapidly progressive interstitial lung disease (RP-ILD) as well as the typical skin lesions of dermatomyositis (DM) without clinical evidence of myositis.(1, 2) The prognosi
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