[Sneddon综合征和抗磷脂抗体:晚期全同源性偏盲的病因]。

M Kriet, A Fiqhi, Y Bouya, S Louaya, A Laktaoui
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引用次数: 0

摘要

斯奈登综合征是一种特殊而罕见的疾病,主要影响年轻女性,其诊断是基于皮肤病变和脑血管缺血发作的共存。它曾被认为是闭塞性血管炎或抗磷脂抗体综合征的表现。我们报告的情况下,一个20岁的女性,谁已经发展了缺血性脑病后的左同名性偏盲。视野检查证实存在完全的左同义性偏视。脑磁共振显示右侧枕脑血管缺血性病变。Sneddon's综合征的诊断是考虑皮肤网状增生和相关的脑缺血事件的存在。通过药物治疗,可以注意到轻微的功能改善,但视野缺陷没有明显改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Sneddon Syndrome and antiphospholipid antibodyies: an etiology of later al homonymous hemianopia].

Sneddon's syndrome is a particular and rare entity that mostly affects young women and whose diagnosis is based on the coexistence of a cuteaneous livedo and a cerebrovascular ischemic attack. It had be considered as being an expression of an occlusive vasculitis or of antiphospholipid antibody syndrome. We report the case of a 20-year-old female, who had developed a left homonymous hemianopia after ischemic encephalopathy. Visual field examination confirmed the presence of a complete left homonymous hemianopia. Cerebral Magnetic Resonance Imaging revealed right occipital cerebrovascular ischemic lesions. Sneddon's syndrome diagnosis was considered on the presence of cutaneous livedo reticularis and associated cerebral ischemic events. With medical treatment, a small functional improvement could be noticed but without net improvement in the visual field defect.

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