Open Access
CC BY 4.0 · Arq Neuropsiquiatr 2024; 82(S 01): S1-S52
DOI: 10.1055/s-0044-1789435
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Optic neuritis as an initial presentation of granulomatosis with polyangiitis: two case reports

Ana Cristina Cotta-Queiroz
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Divisão de Neuro-Oftalmologia, Belo Horizonte MG, Brazil.
,
Anna Christina Higino Rocha
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Divisão de Neuro-Oftalmologia, Belo Horizonte MG, Brazil.
,
Grazielle Fialho Souza
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Divisão de Neuro-Oftalmologia, Belo Horizonte MG, Brazil.
,
Natália Cirino Talim
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Divisão de Neuro-Oftalmologia, Belo Horizonte MG, Brazil.
,
Paulo Pereira Christo
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Divisão de Neuro-Oftalmologia, Belo Horizonte MG, Brazil.
,
Marco A. Lana-Peixoto
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Divisão de Neuro-Oftalmologia, Belo Horizonte MG, Brazil.
› Author Affiliations
 

    Address for correspondence: Marco A. Lana Peixoto (email: marco.lanapeixoto@gmail.com).

    Abstract

    Background: Granulomatosis with polyangiitis (GPA) is a rare systemic vasculitis predominantly involving the respiratory tract and kidneys. While ocular manifestations occur in approximately 50% of the cases, optic neuritis at disease onset is rare. We describe two cases in which optic neuritis was the initial presentation of GPA.

    Case Presentation: Case 1: A 51-year-old, previously healthy man presented with headache and visual loss in the left eye (LE). An examination revealed a visual acuity (VA) of 20/20 in the right eye (RE) and counting fingers in the LE. A relative afferent pupillary defect was observed in the LE. Brain and orbit MRI scans showed pachymeningitis, an expansive lesion in the left orbital apex, and an enhanced lesion in the left optic nerve. The biopsy findings were consistent with GPA. Despite treatment with corticosteroids and cyclophosphamide, he developed loss of vision in the RE. The VA declined to counting fingers in the RE and no light perception in the LE. Case 2: A 56-year-old man developed painful visual loss in the RE. The diagnosis of optic neuritis was made, and he received IV pulses of methylprednisolone, resulting in RE amaurosis. Four months later, he developed painful LE amaurosis with no response to IV methylprednisolone. He was then referred to our center. An examination revealed bilateral amaurosis, ophthalmoplegia in both eyes, and necrotizing scleritis, leading to perforation of the RE. An MRI scan demonstrated bilateral optic nerve enhancement and hyperintense lesions in the apex of both orbits. A biopsy confirmed GPA. No improvement was observed following treatment with cyclophosphamide and steroids. Treatment was subsequently changed to rituximab.

    Conclusion: These cases highlight that optic neuritis may occur at the onset of GPA, contributing to its severe outcomes. Early identification of the nature of the optic neuritis and appropriate treatment are essential to avoid catastrophic outcomes.


    No conflict of interest has been declared by the author(s).

    Publication History

    Article published online:
    02 October 2024

    © 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

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