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Optic nerve involvement in neuro-Behcet's disease.

机译:视神经受累于神经-贝塞特氏病。

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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.
机译:背景:报告神经贝塞特氏病的眼部表现。案例:一名34岁的妇女患有复发性脑膜炎。她出现了复视,头痛和共济失调,并被诊断出患有神经-贝塞特氏病。观察结果:影像学显示在过渡性中脑和脑桥有两个梗塞灶。用泼尼松龙和秋水仙碱治疗后,复视消失。两年后,右眼出现了一个暗点,矫正后的最佳视力为4/200。右眼底可见乳头炎和乳头状前玻璃体混浊。这些发现在结膜下类固醇注射后11天消失,秋水仙碱增加。两个月后,她的视力逐渐提高到20/20。结论:神经-贝塞特氏病可能表现为短暂性视神经炎和乳头状前玻璃体混浊。

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