| Literature DB >> 33033004 |
Izadora Fonseca Zaiden Soares1, Victoria Fernandez Comprido1, Bianca Raquel Ruoh Harn Scovoli Hsu1, Alzira Alves de Siqueira Carvalho2.
Abstract
Subacute symmetrical proximal muscle weakness and persistent elevated creatine kinase levels are typical of immune-mediated necrotising myopathy (IMNM). These conditions are accompanied by copious myofibre necrosis, degeneration and regeneration with minimal to no inflammation on muscle biopsy. We report two cases (case 1 and case 2) of asymptomatic IMNM from different families with hyperCKaemia associated with positive anti-signal recognition particle (SRP) and anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) antibodies, respectively, and we also reviewed the literature. There are only a few previous descriptions of patients with asymptomatic IMNM.The disease onset could be insidious and lead to delayed diagnosis and treatment. We recommend testing for the anti-HMGCR and anti-SRP antibodies in patients with idiopathic hyperCKaemia because they could show no symptoms of this disorder. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: muscle disease; neurology
Mesh:
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Year: 2020 PMID: 33033004 PMCID: PMC7545499 DOI: 10.1136/bcr-2020-235457
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X