2021
DOI: 10.1016/j.jns.2021.120035
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Optic perineuritis: A Canadian case series and literature review

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Cited by 10 publications
(9 citation statements)
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“…Treatment modalities for orbital sarcoidosis include intralesional, oral, and intravenous steroids, methotrexate, cyclosporine, cyclophosphamide, mycophenolate, interferon, azathioprine, hydroxychloroquine, and surgical debulking [1][2][3]6,14]. However, intravenous steroids, which were given in the present case, may be a better option for cases with optic nerve involvement [14].…”
Section: Discussionmentioning
confidence: 76%
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“…Treatment modalities for orbital sarcoidosis include intralesional, oral, and intravenous steroids, methotrexate, cyclosporine, cyclophosphamide, mycophenolate, interferon, azathioprine, hydroxychloroquine, and surgical debulking [1][2][3]6,14]. However, intravenous steroids, which were given in the present case, may be a better option for cases with optic nerve involvement [14].…”
Section: Discussionmentioning
confidence: 76%
“…Other differential diagnoses include metastatic tumors, leukemia, lymphoma, and other orbital inflammatory diseases [3,14]. However, it may be possible to differentiate these diseases, based on the results of blood tests and systemic imaging studies.…”
Section: Discussionmentioning
confidence: 99%
“…OPN is a heterogeneous condition causing inflammation of the optic nerve sheath for which standard treatment is anti-inflammatory or immunosuppressive therapy, usually high-dose corticosteroids. The overwhelming majority of OPN cases have been treated with steroids [ 1 , 3 , 15 ] or, somewhat less commonly, with NSAIDS alone [ 2 ]. It has been suggested that prompt treatment of OPN is essential to avoid poor visual outcomes [ 2 , 16 , 17 ].…”
Section: Discussionmentioning
confidence: 99%
“…He received only lubricating eye drops, and pain subsided at 2-month follow-up. Finally, in a recent Canadian case series, 2 patients were identified as untreated, 1 with idiopathic OPN and normal visual function, and the other with OPN secondary to myelin oligodendrocyte glycoprotein antibody disease and a 2-year history of visual symptoms [ 3 ]. No further details of their workup and clinical course were provided.…”
Section: Discussionmentioning
confidence: 99%
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