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Japanese Journal of Ophthalmology

Optic nerve involvement in neuro-Behcet's disease.

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Toru Nakamura
Kyoichi Takahashi
Shoji Kishi

Nøgleord

Abstrakt

BACKGROUND

To report the ocular manifestations of neuro-Behcet's disease.

METHODS

A 34-year-old woman had recurrent meningitis. She developed diplopia, headache, and ataxia, and was diagnosed as having neuro-Behcet's disease.

METHODS

Imaging revealed two infarct foci in the transitional midbrain and pons. After treatment with prednisolone and colchicine, the diplopia resolved. Two years later, a scotoma developed in the right eye, in which the best-corrected visual acuity was 4/200. Papillitis and a prepapillary vitreous opacity were seen in the right fundus. These findings disappeared 11 days after subconjunctival steroid injections and increased colchicine. Her vision gradually improved to 20/20 two months later.

CONCLUSIONS

Neuro-Behcet's disease may manifest with transient optic neuritis and prepapillary vitreous opacity.

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