Trevisan C, Testa G F, Angelini C
Riv Patol Nerv Ment. 1975 May-Jun;96(3):159-65.
Two cases of progressive supranuclear palsy (PSP) are reported in two men (49 and 75years old) who for one and four years respectively had sudden falling while walking. Rigidity of the neck was an carly feature that prgressed to involve the upper trunk while "subcortical dementia", dysarthria and dysphagia appeared. They had a complete paralysis of vertical eye movements and slow horizontal voluntary eye movements. Oculocephalic reflexes were intact. On caloric stimulation vestibulo-ocular responses were present but only slow saccadic eye movements were observed. With surface electrodes eye movements were studied during the REM phase of sleep. Our patients had both vertical and horizontal eye movements during paradoxal sleep. This findings is in keeping with a supranuclear ophtalmoplegia, and may help in antemorten diagnosis of PSP.
报告了两例进行性核上性麻痹(PSP)病例,患者均为男性,年龄分别为49岁和75岁,他们分别在行走时突然摔倒1年和4年。颈部僵硬是早期特征,随后发展至上躯干,同时出现“皮质下痴呆”、构音障碍和吞咽困难。他们垂直眼球运动完全麻痹,水平随意眼球运动缓慢。眼前庭反射完整。在冷热刺激时存在前庭眼反射,但仅观察到缓慢的眼球扫视运动。使用表面电极在睡眠快速眼动期研究眼球运动。我们的患者在异相睡眠期间有垂直和水平眼球运动。这一发现符合核上性眼肌麻痹,可能有助于进行性核上性麻痹的生前诊断。