2019
DOI: 10.1002/psb.1762
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Management of the idiopathic inflammatory myopathies

Abstract: The idiopathic inflammatory myopathies (IIMs) – comprising polymyositis, dermatomyositis and inclusion body myositis – are a rare group of disorders characterised by muscle inflammation. This article discusses the causes, symptoms, assessment and treatment of these disorders, and the GP's role in management.

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Cited by 6 publications
(4 citation statements)
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“…Dermatomyositis (DM) and polymyositis (PM) are rare, chronic autoimmune connective tissue diseases within the spectrum of the idiopathic inflammatory myopathies (IIMs). 1,2 These conditions are associated with significant disease-related morbidity and mortality.…”
Section: Introductionmentioning
confidence: 99%
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“…Dermatomyositis (DM) and polymyositis (PM) are rare, chronic autoimmune connective tissue diseases within the spectrum of the idiopathic inflammatory myopathies (IIMs). 1,2 These conditions are associated with significant disease-related morbidity and mortality.…”
Section: Introductionmentioning
confidence: 99%
“…1 Disease pathogenesis is complex and incompletely understood; however, ultraviolet radiation (UV) has been implicated in the pathogenesis of DM. 1,4 Treatment is with immunosuppressive medication including glucocorticoids, disease-modifying agents (eg methotrexate and mycophenolate), and often intensive/targeted therapies (eg cyclophosphamide and rituximab). 1,5 However, establishing the diagnosis of IIMs can be challenging, including due to the rarity and heterogeneous manifestations of the spectrum of disease.…”
Section: Introductionmentioning
confidence: 99%
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