Classification tree for subgroups of idiopathic inflammatory myopathies (IIMs). Classification tree for subgroups of idiopathic inflammatory myopathies.

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Autoantibodies in PM and DM Autoantibodies:>90% Autoantibodies:>90% Positive ANA:60-80% Positive ANA:60-80%  More in overlap  Low in IBM Defined antibodies:50%
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Presentation transcript:

Classification tree for subgroups of idiopathic inflammatory myopathies (IIMs). Classification tree for subgroups of idiopathic inflammatory myopathies (IIMs). A patient must first be classified as having IIM using the European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) classification criteria. The patient can then be subclassified using the classification tree. The mixed (dotted outlined box) subgroup of patients with PM includes patients with IMNM. For IBM diagnosis, one of the following, *Finger flexor weakness and response to treatment: not improved or **Muscle biopsy: rimmed vacuoles, is required for diagnosis. ***Juvenile myositis other than JDM was developed based on expert opinion and extrapolation from adults. IMNM and hypomyopathic DM were too few to allow subclassification. ADM, amyopathic dermatomyositis; DM, dermatomyositis; IBM, inclusion body myositis; IMNM, immune-mediated necrotising myopathy; JDM, juvenile dermatomyositis; PM, polymyositis. Matteo Bottai et al. RMD Open 2017;3:e000507 Copyright © BMJ Publishing Group & EULAR. All rights reserved.