Okuma Y, Nagashima T, Hirose K, Tanabe H, Tsubaki T, Mizuno M
Department of Neurology, Tokyo Metropolitan Neurological Hospital, Japan.
No To Shinkei. 1989 Feb;41(2):125-32.
Eleven patients, 7 males and 4 females, of progressive supranuclear palsy (PSP) were examined neuro-otologically for the purpose of elucidating the characteristics of ocular motor abnormalities. All cases were admitted to our hospital and age at onset was from 52 to 71 years old, duration of illness was 2 to 11 years. Range of voluntary eye movements and abnormal eye movements including nystagmus were examined on naked eyes and with electronystagmography (ENG). Smooth pursuit movements and saccadic eye movements were tested both horizontally and vertically by using visual tracking method with ENG recordings. Optokinetic nystagmus test and caloric test with visual suppression test were also performed. These neurotological examinations were made repetitively in 5 cases and their progressions were observed. Vertical gaze palsy and convergence palsy were observed in all cases as the initial symptom. In this study downward gaze was more severely disturbed than upward gaze. Using ENG, saccadic eye movements (saccades) were disturbed earlier than smooth pursuit movements. Hypometric saccades and decreased saccadic velocity were common abnormalities. In the later stage of the disease, horizontal eye movements were also disturbed. In four cases bilateral adduction palsy was added to vertical gaze paralysis so that the lesion of the MLF to oculomotor nucleus was suggested to exist. These voluntary eye movements were worsened gradually as the disease progressed. By using ENG we could find so called abnormal eye movements more frequently than the previous reports. Eight patients demonstrated horizontal gaze nystagmus, and rebound nystagmus were observed in four cases.(ABSTRACT TRUNCATED AT 250 WORDS)
为阐明进行性核上性麻痹(PSP)患者眼动异常的特征,对11例患者(7例男性,4例女性)进行了神经耳科学检查。所有病例均为我院收治,发病年龄52至71岁,病程2至11年。通过裸眼及眼震电图(ENG)检查了自主眼动范围及包括眼球震颤在内的异常眼动。使用ENG记录的视觉跟踪方法,分别在水平和垂直方向测试了平稳跟踪运动和眼球扫视运动。还进行了视动性眼球震颤试验及伴有视觉抑制试验的冷热试验。对5例患者重复进行了这些神经耳科学检查并观察其进展情况。所有病例均以垂直凝视麻痹和集合麻痹作为初始症状。在本研究中,向下凝视比向上凝视受干扰更严重。使用ENG检查时,眼球扫视运动比平稳跟踪运动更早受到干扰。低测眼球扫视和眼球扫视速度降低是常见异常。在疾病后期,水平眼动也受到干扰。4例患者在垂直凝视麻痹基础上又出现双侧内收麻痹,提示中脑导水管周围灰质至动眼神经核存在病变。随着疾病进展,这些自主眼动逐渐恶化。通过使用ENG,我们发现所谓的异常眼动比以往报告更为常见。8例患者出现水平凝视性眼球震颤,4例观察到反弹性眼球震颤。(摘要截选至250词)