170-173 Ozlem ERCEN

نویسندگان

  • Özlem ERÇEN DİKEN
  • Aydın ÇİLEDAĞ
  • Orhan KÜÇÜKŞAHİN
  • Özlem ÖZDEMİR KUMBASAR
چکیده

The idiopathic inflammatory myopathies are a heterogeneous group of rare chronic autoimmune diseases that include polymyositis (PM) and dermatomyositis (DM). Antisynthetase syndrome (ASS) is recognized as a subset of the idiopathic inflammatory myopathies and the syndrome is characterized by myositis associated with interstitial lung disease (ILD) and autoantibodies against aminoacyl-tRNA synthetases (ARS) with anti-Jo-1 being the most commonly found antibody (1,2). ILD is occurred in 70-89% of patients and it is the most common manifestation of ASS (3,4). In a subgroup of patients, without myositis the ILD may dominate the clinical manifestation and it is termed as amyopathic ASS (2).

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تاریخ انتشار 2013