Optic nerve involvement in neuro-Behcet's disease.

Jpn J Ophthalmol

Department of Ophthalmology, Gunma University School of Medicine, Maebashi, Japan.

Published: April 2002

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

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

Observations: 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.

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

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http://dx.doi.org/10.1016/s0021-5155(01)00466-xDOI Listing

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