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Polymyositis: The Comet Tail After COVID-19
Said Amin1,2, Fawad Rahim1,2, Mohammad Noor1,2
1Internal Medicine, Khyber Girls Medical College, Peshawar, PAK.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can trigger autoimmune disorders like polymyositis. This case highlights a patient’s recovery from COVID-19-related inflammatory myopathy with targeted treatment.
Area of Science:
- Rheumatology
- Infectious Diseases
- Neurology
Background:
- Infectious agents, including SARS-CoV-2, are increasingly implicated in autoimmune disorders.
- SARS-CoV-2, initially viewed as a respiratory pathogen, is now associated with various autoimmune rheumatic conditions.
- The pathogenesis of muscle injury in COVID-19 is often attributed to autoimmune inflammatory damage or cytokine storm.
Observation:
- A 52-year-old female presented with significant muscle weakness (MRC grade 3/5), body aches, and fatigue four months post-mild COVID-19.
- Clinical presentation included proximal muscle weakness and elevated muscle enzymes.
- Diagnostic workup revealed an active myopathic process on electromyography and inflammatory myopathy on muscle biopsy.
Findings:
- The patient was diagnosed with inflammatory polymyositis secondary to COVID-19.
- Treatment with prednisolone and azathioprine led to a remarkable recovery of muscle strength to MRC grade 5/5 within four weeks.
- This case adds to the limited reports of inflammatory polymyositis post-COVID-19, particularly in developing regions.
Implications:
- This case underscores the potential for SARS-CoV-2 to induce delayed-onset autoimmune inflammatory myopathy.
- Early diagnosis and immunosuppressive therapy can lead to significant functional recovery.
- Further research is needed to elucidate the precise mechanisms linking SARS-CoV-2 to autoimmune myopathies.
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