| Literature DB >> 35273416 |
Daniela Ximena Rojas-Correa1, José Alberto Reche-Sainz1, Alfredo Insausti-García1, Cristina Calleja-García1, Manuel Ferro-Osuna1.
Abstract
Neurological manifestations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are relatively common. Although some may be consequences of direct cellular viral invasion (neurotropism), many represent post-infectious inflammation mediated by autoimmune mechanisms. We herein report the case of a 69-year-old diabetic male who presented with bilateral sub-acute, progressive loss of vision 45 days after suffering a presumed SARS-CoV-2 related pneumonia. He had bilateral optic disc oedema. Magnetic resonance imaging showed uniform contrast enhancement of both optic nerves without spinal cord involvement. He tested positive for SARS-CoV-2 IgG and myelin oligodendrocyte glycoprotein (MOG) IgG antibodies. He was treated with intravenous methylprednisolone for 5 days. The optic disc oedema resolved within 6 weeks with improvement in visual acuity, although optic atrophy developed by week 16. The MOG-IgG antibody test turned negative after 24 weeks.Entities:
Keywords: COVID-19; SARS-CoV-2; myelin oligodendrocyte glycoprotein (MOG); optic neuritis
Year: 2021 PMID: 35273416 PMCID: PMC8903772 DOI: 10.1080/01658107.2021.1916044
Source DB: PubMed Journal: Neuroophthalmology ISSN: 0165-8107