Related Experiment Video
Updated: Sep 2, 2025

Author Spotlight: Unveiling the Polyfunctionality and Heterogeneity in Immune Responses
Published on: March 8, 2024
Polymyositis: The Comet Tail After COVID-19
Said Amin1,2, Fawad Rahim1,2, Mohammad Noor1,2
1Internal Medicine, Khyber Girls Medical College, Peshawar, PAK.
Abstract:
Infectious agents have been implicated in the pathogenesis of autoimmune disorders for decades. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is no exception. This became evident as the pandemic evolved. Once considered a respiratory pathogen only, SARS-CoV-2 is now linked to a variety of autoimmune rheumatic disorders such as rheumatoid arthritis, systemic lupus erythematosus, reactive arthritis, spondyloarthropathies, vasculitis, and inflammatory myopathy. Although the exact cause for muscle injury in the setting of coronavirus disease 2019 (COVID-19) is not established, autoimmune inflammatory damage is the most accepted mechanism. Moreover, SARS-CoV-2 can cause direct muscle damage and indirectly through a cytokine storm. Inflammatory polymyositis in relation to COVID-19 has seldom been reported in developing countries. Here, we report a unique case of inflammatory polymyositis in a 52-year-old lady. The patient presented with muscle weakness, generalized body aches, and fatigue occurring four months after recovering from mild COVID-19. She had muscle weakness of Medical Research Council (MRC) grade 3/5 involving the shoulders and pelvic girdle with elevated muscle enzymes. Electromyography revealed an active irritable myopathic process consistent with inflammatory polymyositis. She underwent magnetic resonance imaging-guided muscle biopsy from the right thigh which revealed findings consistent with inflammatory myopathy. She was offered prednisolone and azathioprine. After four weeks of treatment, she had a remarkable improvement in her muscle strength to MRC grade 5/5.
Insights
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.
Related Concept Videos
Myocarditis II: Clinical Features and Diagnostic Tests
Myocarditis III: Medical Management
Myocarditis I: Introduction
Myocarditis IV: Nursing Management
Myasthenia Gravis: Overview and Treatment
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which...
Myasthenia Gravis: Diagnostic Tests
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...

