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Seronegative Immune-Mediated Necrotizing Myopathy: A Case Report
Shriya Patel1, Mohammad Abu-Abaa2, Feryal Mousavi2
1Department of Internal Medicine, Rowan University School of Osteopathic Medicine, Stratford, USA.
This case study highlights immune-mediated necrotizing myopathy (IMNM), a subtype of idiopathic inflammatory myopathies. Early corticosteroid treatment followed by azathioprine significantly improved muscle strength in a statin-using patient.
Area of Science:
- Rheumatology
- Neurology
- Immunology
Background:
- Idiopathic inflammatory myopathies (IIMs) encompass autoimmune disorders causing muscle weakness.
- Immune-mediated necrotizing myopathy (IMNM) is a specific IIM subtype.
- IMNM classification includes autoantibodies like anti-HMGCR and anti-SRP, or seronegative status.
Observation:
- A 61-year-old female with a history of lung cancer and current statin use presented with subacute proximal lower extremity weakness.
- Laboratory tests revealed markedly elevated creatinine kinase (CK) and amino transaminases.
- The patient exhibited bilateral proximal lower extremity muscle weakness.
Findings:
- Initial inpatient treatment with corticosteroids led to successful outcomes.
- Corticosteroids were discontinued and azathioprine was initiated three months post-admission.
- The patient achieved a 60% increase in muscle strength after treatment.
Implications:
- This case underscores the importance of recognizing IMNM in patients with risk factors like statin use.
- Effective management strategies involving immunosuppressive therapy can lead to significant clinical improvement.
- Further research into IMNM pathogenesis and treatment is warranted.
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