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Article Synopsis
  • - The study analyzed clinical characteristics and prognostic factors of patients with idiopathic inflammatory myopathy (IIM) who also had interstitial lung disease (ILD) and included 39 males and 111 females with a mean onset age of 50.4 years and a median disease duration of 3 months.
  • - Among the patients, 97 had dermatomyositis (DM-ILD) and 53 had antisynthetase syndrome (ASS-ILD), with DM-ILD patients showing higher rates of anti-MDA5 antibodies and common symptoms such as skin ulcers and rapidly progressing ILD, while ASS-ILD patients showed higher rates of anti-Jo-1 antibodies and pericardial effusion.
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  • Idiopathic inflammatory myopathies (IIMs) are unique autoimmune disorders causing muscle weakness and additional symptoms, with recent criteria defining their subgroups for better classification.
  • This study involved 90 IIM patients and a control group, assessing nailfold capillaroscopy (NFC) patterns and their correlation with clinical signs to identify diagnostic potential across different IIM types.
  • Results showed a high incidence of scleroderma capillaroscopic patterns in dermatomyositis and amyopathic dermatomyositis, indicating NFC's usefulness in discerning IIM subtypes and linking them to specific clinical features.
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