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Clinical features of anti-MOG antibody-positive optic neuritis at Tokushima University Hospital Takafumi Misaki 1 , Mariko Egawa 1 , Yoshinori Mitamura 1 1Department of Ophthalmology, Institute of Biomedical Sciences, Tokushima University Graduate School pp.734-740
Published Date 2024/6/15
DOI https://doi.org/10.11477/mf.1410215199
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Abstract Purpose:To report the clinical features of anti-MOG antibody-positive optic neuritis(MOG-ON).

Subject and method:We examined the clinical characteristics of 15 eyes of 10 patients diagnosed with MOG-ON at Tokushima University Hospital from June 2017 to April 2023.

Results:The average age at onset was 36.6±25.1 years(three patients were aged below 15 years);five patients were male and five were female. Further, five cases were unilateral and five were bilateral. Subjective symptoms at onset were eye pain in seven patients cases and headache in four patients. Three patients had fever and two had dysuria, and the most common visual field disorder was central scotoma in eight eyes. Swelling of the entire length of the optic nerve was observed in all patients on MRI examination. Extraocular lesions included myelitis in one case and Acute disseminated encephalomyelitis in all cases in the pediatric group. Steroid pulse therapy was performed in all cases, with immunoglobulin therapy in two cases, blood purification therapy in one case, and a combination of both in one case. The mean logMAR visual acuity was markedly improved from 1.12±0.69 at the initial examination to −0.13±0.06 after treatment, and visual field defects disappeared. Oral prednisolone was administered as maintenance therapy, and recurrence was observed in three patients.

Conclusion:Eye pain and lesions extending along the entire length of the optic nerve were observed at a high rate. Although the final visual acuity after treatment was good, frequent pulse therapy and combination therapy were required in the pediatric group. Recurrence is common, and long-term follow-up is required.


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