| Literature DB >> 29691272 |
Emily Liang1, Mandana Rastegar2,3.
Abstract
Immune-mediated necrotising myopathy (IMNM) is a type of inflammatory myopathy characterised by acute or subacute severe proximal muscle weakness, significantly elevated creatine kinase levels, and prominent myofibre necrosis and regeneration with little or no inflammation. A subtype of IMNM identified by anti-HMG-CoA reductase (HMGCR)antibodies has been shown to be associated with statin exposure. Treatment of IMNM consists of immunosuppression with steroids, steroid-sparing agents, intravenous immune globulin and/or biologics. We present here a case of anti-HMCGR-associated IMNM and review the pathophysiology, diagnosis and treatment to increase physician awareness of this rare and debilitating condition. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: disability; muscle disease; musculoskeletal and joint disorders; musculoskeletal syndromes
Mesh:
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Year: 2018 PMID: 29691272 PMCID: PMC5926624 DOI: 10.1136/bcr-2017-223870
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X