An overview of the idiopathic inflammatory myopathies

Published on January 30, 2017   36 min

Other Talks in the Series: Topical Talks

0:00
My name is Jemima Albayda. I'm an Assistant Professor at the Johns Hopkins University, seeing patients at the Division of Rheumatology, Myositis Center. Today, I will give you "An overview of the Idiopathic Inflammatory Myopathies".
0:17
Our objectives with this talk are to describe the clinical presentation of the idiopathic inflammatory myopathies. To define the subgroups of myositis. And present the framework for current understanding of classification. To enumerate the known antibody associations. And discuss how they help guide prognosis and management. To detail the clinical evaluation of myositis and the role of ancillary testing. And to briefly discuss treatment strategies.
0:47
The idiopathic inflammatory myopathies are a rare group of acquired autoimmune muscle disorders. Clinically, they are characterized by muscle weakness and by inflammatory cell infiltrates in the muscle. Although, it is thought of as a muscle disorder, it is quite heterogenous in presentation and treatment response. Extramuscular manifestations are often seen and can include skin and lung inflammation, joint, heart, and rarely GI tract involvement. There's also a known increased risk of malignancy, particularly, in cases of dermatomyositis.
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An overview of the idiopathic inflammatory myopathies

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