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Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient

PURPOSE: SARS‐CoV‐2 viral infection affects multiple systems including the respiratory, gastrointestinal, neurological, cardiac, and ophthalmic systems. We report a case of myelin oligodendrocyte glycoprotein (MOG) related optic neuritis in a SARS‐CoV‐2 (COVID‐19) patient. METHODS: Case report. RESU...

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Autores principales: Zaini, Mohamad Azlan, Mohd Zain, Ayesha, Md Din, Norshamsiah, Lam, Chenshen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599276/
https://www.ncbi.nlm.nih.gov/pubmed/37904693
http://dx.doi.org/10.1002/iid3.1051
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author Zaini, Mohamad Azlan
Mohd Zain, Ayesha
Md Din, Norshamsiah
Lam, Chenshen
author_facet Zaini, Mohamad Azlan
Mohd Zain, Ayesha
Md Din, Norshamsiah
Lam, Chenshen
author_sort Zaini, Mohamad Azlan
collection PubMed
description PURPOSE: SARS‐CoV‐2 viral infection affects multiple systems including the respiratory, gastrointestinal, neurological, cardiac, and ophthalmic systems. We report a case of myelin oligodendrocyte glycoprotein (MOG) related optic neuritis in a SARS‐CoV‐2 (COVID‐19) patient. METHODS: Case report. RESULTS: A 36‐year‐old Malay gentleman with underlying hypertension presented with the first episode of bilateral progressively worsening blurred vision for 1 week associated with retrobulbar pain. There were no other neurological symptoms. He had fever a week before the eye symptoms and tested positive for COVID‐19. He received COVID‐19 booster vaccine a month before the disease onset. On examination, his vision was hand motion on right eye and 6/18 on left eye. Relative afferent pupillary defect (RAPD) was positive on right eye with abnormal optic nerve function tests. Anterior segments were unremarkable. Fundus examination showed bilateral optic disc swelling. MRI revealed multifocal hyperintense subcortical white matter lesions. Optic nerves appeared normal with no enhancement seen. Blood investigation showed a positive serum MOG antibody. Intravenous methylprednisolone was commenced followed by oral prednisolone after which his vision and ocular symptoms markedly improved. The oral prednisolone was tapered alongside addition of azathioprine. At 1 month, the disease was stable with no recurrence. CONCLUSION: While optic neuritis has been associated with both COVID‐19 infection and vaccination, MOG IgG antibody‐mediated optic neuritis is also a possible manifestation. This type of optic neuritis associated with COVID‐19 infection does not show a similar pattern of frequent recurrences as seen in non‐COVID‐19 related optic neuritis.
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spelling pubmed-105992762023-10-26 Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient Zaini, Mohamad Azlan Mohd Zain, Ayesha Md Din, Norshamsiah Lam, Chenshen Immun Inflamm Dis Letter PURPOSE: SARS‐CoV‐2 viral infection affects multiple systems including the respiratory, gastrointestinal, neurological, cardiac, and ophthalmic systems. We report a case of myelin oligodendrocyte glycoprotein (MOG) related optic neuritis in a SARS‐CoV‐2 (COVID‐19) patient. METHODS: Case report. RESULTS: A 36‐year‐old Malay gentleman with underlying hypertension presented with the first episode of bilateral progressively worsening blurred vision for 1 week associated with retrobulbar pain. There were no other neurological symptoms. He had fever a week before the eye symptoms and tested positive for COVID‐19. He received COVID‐19 booster vaccine a month before the disease onset. On examination, his vision was hand motion on right eye and 6/18 on left eye. Relative afferent pupillary defect (RAPD) was positive on right eye with abnormal optic nerve function tests. Anterior segments were unremarkable. Fundus examination showed bilateral optic disc swelling. MRI revealed multifocal hyperintense subcortical white matter lesions. Optic nerves appeared normal with no enhancement seen. Blood investigation showed a positive serum MOG antibody. Intravenous methylprednisolone was commenced followed by oral prednisolone after which his vision and ocular symptoms markedly improved. The oral prednisolone was tapered alongside addition of azathioprine. At 1 month, the disease was stable with no recurrence. CONCLUSION: While optic neuritis has been associated with both COVID‐19 infection and vaccination, MOG IgG antibody‐mediated optic neuritis is also a possible manifestation. This type of optic neuritis associated with COVID‐19 infection does not show a similar pattern of frequent recurrences as seen in non‐COVID‐19 related optic neuritis. John Wiley and Sons Inc. 2023-10-25 /pmc/articles/PMC10599276/ /pubmed/37904693 http://dx.doi.org/10.1002/iid3.1051 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter
Zaini, Mohamad Azlan
Mohd Zain, Ayesha
Md Din, Norshamsiah
Lam, Chenshen
Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient
title Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient
title_full Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient
title_fullStr Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient
title_full_unstemmed Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient
title_short Myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐COVID‐19 infection patient
title_sort myelin oligodendrocyte glycoprotein antibody‐associated optic neuritis in a post‐covid‐19 infection patient
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599276/
https://www.ncbi.nlm.nih.gov/pubmed/37904693
http://dx.doi.org/10.1002/iid3.1051
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