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[Muscle weakness and CK elevation: is it myositis?]
A Kernder1, J Mucke2, A-S Moldovan3
1Poliklinik für Rheumatologie und Hiller Forschungszentrum, Universitätsklinikum Düsseldorf, Moorenstr. 5, 40225, Düsseldorf, Deutschland. annaluise.kernder@med.uni-duesseldorf.de.
Muscle biopsy is crucial for diagnosing rare myopathies. Two cases highlight immune-mediated necrotizing myopathy (IMNM) from statins and myoadenylate deaminase deficiency, even with normal creatine kinase (CK) levels.
Area of Science:
- Neurology
- Rheumatology
- Genetics
Background:
- Rheumatologists frequently encounter patients with muscle weakness and elevated creatine kinase (CK) levels.
- Diagnosing the specific cause of myopathy can be challenging, as myositis is not always the underlying condition.
- Muscle biopsy is an essential diagnostic tool when initial evaluations are inconclusive.
Observation:
- Case 1: A patient presented with severe muscle weakness, pathological weight loss, and significantly elevated CK levels.
- Case 2: Another patient experienced cramp-like and burning muscle pain with limb weakness, but without markedly increased CK levels.
Findings:
- Muscle biopsy in Case 1 revealed immune-mediated necrotizing myopathy (IMNM) associated with anti-3-hydroxy-3-methyl-glutaryl-CoA reductase (HMG-CoA reductase) autoantibodies, likely induced by statin use.
- Muscle biopsy in Case 2 identified myoadenylate deaminase deficiency, a diagnosis further confirmed by genetic testing.
Implications:
- These cases underscore the diagnostic utility of muscle biopsy in identifying specific myopathies, including statin-induced IMNM and myoadenylate deaminase deficiency.
- The findings emphasize that elevated CK levels are not always present in all myopathies, necessitating alternative diagnostic approaches.
- Accurate diagnosis through muscle biopsy and genetic testing is critical for appropriate patient management and treatment strategies in rheumatology and neurology.
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