COVID-19-Associated MDA5-Mediated Necrotizing Myositis

Sarah Steadman1, Amit Sikder2, Harsh R Desai3

  • 1Edward Via College of Osteopathic Medicine-Carolinas Campus, Spartanburg, SC, USA.

PubMed

Insights

This case report details a rare instance of autoimmune myositis linked to SARS-CoV-2 infection. Early diagnosis of COVID-19-related myopathies is crucial for effective treatment and improved patient outcomes.

Area of Science:

  • Neurology
  • Immunology
  • Infectious Diseases

Background:

  • Rhabdomyolysis and autoimmune myopathies share symptoms like muscle pain and weakness, complicating diagnosis.
  • The SARS-CoV-2 pandemic has seen a rise in reported autoimmune myositis cases.
  • Distinguishing viral-induced muscle damage from autoimmune conditions is clinically challenging.

Purpose of the Study:

  • To report the first case of melanoma differentiation-associated gene 5 (MDA5)-associated necrotizing myositis following SARS-CoV-2 infection.
  • To highlight a unique presentation of COVID-19-related myopathy without typical skin or lung involvement.
  • To emphasize the diagnostic challenges and treatment response in post-viral autoimmune myopathies.

Main Methods:

  • Clinical case presentation of a young African American male with post-SARS-CoV-2 myopathy.
  • Diagnostic workup including serum creatine kinase (CK) levels, inflammatory markers, autoimmune panel, and chest CT.
  • Treatment assessment with intravenous fluids and empiric steroid therapy.
  • Confirmation via muscle biopsy and specific antibody testing (MDA5).

Main Results:

  • Patient presented with severe myalgias and weakness post-COVID-19, with markedly elevated CK levels (>300,000 U/L).
  • Initial treatment for rhabdomyolysis yielded poor results, but empiric steroids led to rapid symptom and CK level improvement.
  • Muscle biopsy confirmed necrotizing myositis, and elevated MDA5 antibodies were detected.
  • The patient lacked typical MDA5-related skin and interstitial lung disease manifestations.

Conclusions:

  • This is the first reported case of MDA5-associated necrotizing myositis triggered by SARS-CoV-2 infection.
  • The absence of characteristic skin and lung findings in this patient broadens the clinical spectrum of MDA5 myositis.
  • Further research is essential to understand COVID-19's role in autoimmune myopathies and develop targeted treatments.

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