罕见的埃文斯综合征合并视神经炎1例

Miranda Dbd
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摘要

目的:报告1例埃文斯综合征合并严重视神经炎。病例报告:HAF,男,26岁,9岁时被诊断为Evans综合征,有头痛和右眼疼痛史,运动恶化。初始状态15天后,视力开始浑浊,视力下降。眼科检查显示右眼视力为20/200,随病情进展逐渐恶化;左眼视力恢复正常。右眼有绝对暗点,左眼各象限有相对和绝对暗点。葡萄糖素血管造影结果包括视盘衰减,无高荧光病变。结论:Evans综合征是一种临床研究领域逐渐扩大的病理,其发病机制及其与其他合并症的关联有了新的概念。在这种情况下,我们报告与单侧视神经炎的关系,负责进行性视力丧失。这些知识汇集了科学界,并转化为早期多学科方法的需要。
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A Rare Case of Evans Syndrome Associated With Optic Neuritis: A Case Report
Purpose: To report a case of Evans Syndrome associated with severe optic neuritis. Case Report: HAF, male, 26 years old, diagnosed with Evans Syndrome at the age of nine, with a history of headache and right eye pain with worsening movement. Fifteen days after the initial condition, visual clouding and decreased visual acuity began. Ophthalmological examination revealed visual acuity of 20/200 in the right eye with progressive worsening as the condition progressed; and 20/20 in the left eye. Visual field with absolute scotomata in the right eye and relative and absolute scotomatous points in all quadrants of the left eye. Gluorescein angiography findings included optic disc attenuation, without hyperfluorescent lesions. Conclusion: Evans Syndrome is a pathology that is gradually expanding in the field of clinical research, which has allowed new concepts related to pathogenesis and association with other comorbid conditions. In this case, we report the association with unilateral Optic Neuritis, responsible for progressive visual loss. Such knowledge aggregates the scientific community and translates into the need for an early multidisciplinary approach.
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