Appearance of anti-acetylcholine receptor antibodies after COVID-19

Objectives: In this paper, we report a case of Myasthenia Gravis (MG) exacerbated by COVID-19 that was initially anti-acetylcholine receptor (AChR) negative and after 9 months became positive for anti-AChR antibodies. Methods: We performed a review of the medical records and clinical follow-up of a patient followed at the Neurology service of Walter Cantídio University Hospital. Results: A 37-year-old female patient presented with mild dysphonia, ptosis and diplopia. Three months later, she was admitted to the hospital with respiratory failure associated with COVID-19. The patient received a clinical diagnosis of MG and anti-AChR and MuSK antibodies were negative at that moment. Nine months after initial presentation, serum anti-AChR antibodies were positive. Conclusion: We reported a patient who presented seroconversion for anti-AChR antibodies after COVID-19. There have been some reports of possible viral triggers for myasthenia, but controversy over this matter still remains.

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Publication Details

Journal
Revista de Medicina da UFC
Published
2025-05-02
DOI
https://doi.org/10.20513/2447-6595.2025v65n1e90635
Primary Topic
Peripheral Neuropathies and Disorders
Type
article
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article

Appearance of anti-acetylcholine receptor antibodies after COVID-19

Walisson Grangeiro Bringel Silva, Hermany Capistrano Freitas, Paulo Ribeiro Nóbrega, Cleonísio Leite Rodrigues et al.
Revista de Medicina da UFC
Peripheral Neuropathies and Disorders
article

Appearance of anti-acetylcholine receptor antibodies after COVID-19

Walisson Grangeiro Bringel Silva, Hermany Capistrano Freitas, Paulo Ribeiro Nóbrega, Cleonísio Leite Rodrigues, Pedro Helder de Oliveira
article en

Abstract

Objectives: In this paper, we report a case of Myasthenia Gravis (MG) exacerbated by COVID-19 that was initially anti-acetylcholine receptor (AChR) negative and after 9 months became positive for anti-AChR antibodies. Methods: We performed a review of the medical records and clinical follow-up of a patient followed at the Neurology service of Walter Cantídio University Hospital. Results: A 37-year-old female patient presented with mild dysphonia, ptosis and diplopia. Three months later, she was admitted to the hospital with respiratory failure associated with COVID-19. The patient received a clinical diagnosis of MG and anti-AChR and MuSK antibodies were negative at that moment. Nine months after initial presentation, serum anti-AChR antibodies were positive. Conclusion: We reported a patient who presented seroconversion for anti-AChR antibodies after COVID-19. There have been some reports of possible viral triggers for myasthenia, but controversy over this matter still remains.

Revista de Medicina da UFCVol. 65
Universidade Federal do Ceará (BR), Hospital Geral de Fortaleza (BR)
Openalex Percentile: Top 84%
Peripheral Neuropathies and Disorders
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