Inflammatory myopathy: Difference between revisions

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**Juvenile dermatomyositis
**Juvenile dermatomyositis


==Differential Diagnosis==
==Differentiating Inflammatory Myopathy from other Diseases==


==References==
==References==
{{reflist|2}}
{{reflist|2}}

Revision as of 16:36, 6 April 2018

Inflammatory Myopathy

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Overview

Classification

Differentiating Inflammatory myopathy from other Diseases

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]

Overview

Classification

  • The 2017 European League Against Rheumatism and American College of Rheumatology (EULAR/ACR) classified idiopathic inflammatory myopathy into 6 subtypes:[1][2]
    • Polymyositis
    • Dermatomyositis
    • Inclusion body myositis
    • Immune-mediated necrotizing myopathies (IMNM)
    • Amyopathic dermatomyositis
    • Juvenile dermatomyositis

Differentiating Inflammatory Myopathy from other Diseases

References

  1. Leclair V, Lundberg IE (March 2018). "New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter". Curr Rheumatol Rep. 20 (4): 18. doi:10.1007/s11926-018-0726-4. PMC 5857275. PMID 29550929.
  2. Lundberg IE, Tjärnlund A, Bottai M, Werth VP, Pilkington C, Visser M, Alfredsson L, Amato AA, Barohn RJ, Liang MH, Singh JA, Aggarwal R, Arnardottir S, Chinoy H, Cooper RG, Dankó K, Dimachkie MM, Feldman BM, Torre IG, Gordon P, Hayashi T, Katz JD, Kohsaka H, Lachenbruch PA, Lang BA, Li Y, Oddis CV, Olesinska M, Reed AM, Rutkowska-Sak L, Sanner H, Selva-O'Callaghan A, Song YW, Vencovsky J, Ytterberg SR, Miller FW, Rider LG (December 2017). "2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups". Ann. Rheum. Dis. 76 (12): 1955–1964. doi:10.1136/annrheumdis-2017-211468. PMID 29079590.