Paracentral Acute Middle Maculopathy Associated with Severe Anti-Mog (Myelin Oligodendrocyte Glycoprotein)-Positive Optic Neuritis.
Autor: | Fernandes RD; Division of Ophthalmology and the Laboratory of Investigation in Ophthalmology (LIM 33), University of São Paulo Medical School, São Paulo, Brazil., de Souza Andrade T; Division of Ophthalmology and the Laboratory of Investigation in Ophthalmology (LIM 33), University of São Paulo Medical School, São Paulo, Brazil., Preti RC; Division of Ophthalmology and the Laboratory of Investigation in Ophthalmology (LIM 33), University of São Paulo Medical School, São Paulo, Brazil., Zacharias LC; Division of Ophthalmology and the Laboratory of Investigation in Ophthalmology (LIM 33), University of São Paulo Medical School, São Paulo, Brazil., Silva GD; Department of Neurology, University of São Paulo Medical School, São Paulo, Brazil., Lucato LT; Neuroradiology Section, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil., Apóstolos-Pereira SL; Department of Neurology, University of São Paulo Medical School, São Paulo, Brazil., Callegaro D; Department of Neurology, University of São Paulo Medical School, São Paulo, Brazil., Monteiro MLR; Division of Ophthalmology and the Laboratory of Investigation in Ophthalmology (LIM 33), University of São Paulo Medical School, São Paulo, Brazil. |
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Jazyk: | angličtina |
Zdroj: | Neuro-ophthalmology (Aeolus Press) [Neuroophthalmology] 2023 Feb 01; Vol. 47 (3), pp. 156-163. Date of Electronic Publication: 2023 Feb 01 (Print Publication: 2023). |
DOI: | 10.1080/01658107.2023.2172434 |
Abstrakt: | Retinal complications in patients with inflammatory optic neuritis (ON) are generally related to post-infectious neuroretinitis and are considered uncommon in autoimmune/demyelinating ON, whether isolated or caused by multiple sclerosis (MS) or neuromyelitis optica spectrum disorder (NMOSD). More recently, however, cases with retinal complications have been reported in subjects positive for myelin oligodendrocyte glycoprotein (MOG) antibodies. We report a 53-year-old woman presenting with severe bilateral ON associated with a focal area of paracentral acute middle maculopathy (PAMM) in one eye. Visual loss recovered remarkably after high-dose intravenous corticosteroid treatment and plasmapheresis, but the PAMM lesion remained visible on both optical coherence tomography and angiography as an ischaemic lesion affecting the middle layers of the retina. The report emphasises the possible occurrence of retinal vascular complications in MOG-related optic neuritis, an important addition to the diagnosis of, and possible differentiation from, MS-related or NMOSD-related ON. Competing Interests: No potential conflict of interest was reported by the authors. (© 2023 Taylor & Francis Group, LLC.) |
Databáze: | MEDLINE |
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