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Temporal association between SARS-CoV-2 and new-onset myasthenia gravis: is it causal or coincidental?
Y Muralidhar Reddy1, Santhosh Kumar B2, Syed Osman2
1Neurology, Care Hospital Banjara Hills, Hyderabad, India muralidharnims@gmail.com.
Abstract:
Several case reports of COVID-19 in patients with myasthenia gravis (MG) have been documented. However, new-onset autoimmune MG following COVID-19 has been reported very rarely. We report one such case here. A 65-year-old man presented to us with dysphagia 6 weeks following mild COVID-19. He was evaluated and diagnosed as antiacetylcholine receptor antibody (AchR) positive, non-thymomatous, generalised MG. He subsequently developed myasthenic crisis and improved after treatment with intravenous immunoglobulin, prednisolone and pyridostigmine. Systematic literature review showed eight more similar cases. Analysis of all cases including the one reported here showed these features: mean age 55.8 years, male gender (5), time interval between COVID-19 and MG (5-56 days), generalised (5), bulbar and/or ocular symptoms (4), anti-AchR antibodies (7) and antimuscle-specific kinase antibodies (2). All have improved with immunotherapy. Although, many hypothesis are proposed to explain causal relationship between the two, it could as well be sheer coincidence.
Insights
New-onset autoimmune myasthenia gravis (MG) following COVID-19 is rare. This case report and literature review highlight key features and treatment responses in patients experiencing MG after SARS-CoV-2 infection.
Area of Science:
- Neurology
- Infectious Diseases
- Immunology
Background:
- Myasthenia gravis (MG) is a rare autoimmune disorder affecting neuromuscular junctions.
- While COVID-19 has been documented in MG patients, new-onset autoimmune MG post-COVID-19 is exceptionally uncommon.
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