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review-article

Imaging in dermatomyositis in adults and children

Introduction Dermatomyositis (DM) is a rare systemic autoimmune disorder in which an abnormal immune reaction against vascular endothelial antigens and endomysium appears to lead to obstructive inflammatory changes of blood vessels within muscles, skin and other tissues(1). DM belongs to the group of idiopathic inflammatory myopathies (IIM) which according to the recent EULAR/ACR classification criteria, can be classified into six subgroups: polymyositis (PM), inclusion body myositis (IBM

Iwona Sudoł-Szopińska, Thibaut Jacques, Piotr Gietka, Anne Cotten

Journal of Ultrasonography , ISSUE 80, 36–42

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