Gomori A J, Sima A A
Can J Neurol Sci. 1984 Feb;11(1):48-52. doi: 10.1017/s0317167100045315.
We report a 59 year old woman who presented with double vision, nuchal pain and mild dementia. On neurological examination she demonstrated third, sixth and seventh nerve palsies and ataxia. Following intravenous ACTH and oral prednisone therapy she showed a remarkable recovery which left her with only a left facial weakness. She remained well for two years. She then developed bulbar palsy and profound dementia. Pathological examination revealed progressive supranuclear palsy (PSP). This patient demonstrated a greater variability in the course of PSP than has previously been recognized.
我们报告了一名59岁女性,她出现复视、颈部疼痛和轻度痴呆。神经系统检查显示她有动眼神经、展神经和面神经麻痹以及共济失调。在接受静脉注射促肾上腺皮质激素(ACTH)和口服泼尼松治疗后,她有显著恢复,仅遗留左侧面部无力。她两年情况良好。之后她出现球麻痹和严重痴呆。病理检查显示为进行性核上性麻痹(PSP)。该患者PSP病程的变异性比之前认识到的更大。