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ABSTRACT: Objectives
The clinicopathological features of immune-mediated necrotizing myopathy (IMNM) sometimes mimic muscular dystrophy, complicating accurate diagnosis. The European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) classification criteria of idiopathic inflammatory myopathies (IIMs) are superior in terms of sensitivity and specificity; however, the sensitivity is reported to be relatively low in IMNM. We examined the clinicopathological characteristics and the prognoses of anti-3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) antibody-positive and anti-signal recognition particle (SRP) antibody-positive cases that do not satisfy the EULAR/ACR classification criteria.Methods
Seventy-one anti-HMGCR antibody-positive cases and 94 anti-SRP antibod
SUBMITTER: Komaki S
PROVIDER: S-EPMC12316373 | biostudies-literature | 2025 Aug
REPOSITORIES: biostudies-literature