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Title: [PM-Scl antibody positive systemic sclerosis associated with inclusion-body myositis]. Author: Kim S, Genth E, Krieg T, Hunzelmann N. Journal: Z Rheumatol; 2005 Oct; 64(7):499-502. PubMed ID: 16244833. Abstract: We describe a 72- year-old patient with a ten year history of anti-PM-Scl positive systemic sclerosis associated with inclusion-body myositis. While the association of dermatomyositis and polymyositis with anti-PM-Scl positive systemic sclerosis is frequently reported, inclusion-body myositis was, to the best of our knowledge, only previously described once in association with anti-PM-Scl-positive systemic sclerosis. The distinction between inclusion-body myositis and other forms of inflammatory myopathy, like the histopathologically well distinguishable polymyositis or dermatomyositis, is relevant because of the poor response of inclusion- body myositis to immunosuppressive treatment. Our case underlines that in patients with anti-PM-Scl-positive systemic sclerosis and treatment resistant progressive myopathy the diagnosis of inclusion body myositis should be considered.[Abstract] [Full Text] [Related] [New Search]