Wessel K, Huss G P, Brückmann H, Kömpf D
Klinik für Neurologie, Medizinsche Universität zu Lübeck, Germany.
J Neurol. 1993;240(3):168-76. doi: 10.1007/BF00857523.
The follow-up of neurophysiological tests (brain-stem auditory evoked potentials; blink reflex; sensory, motor and visual evoked potentials) and CT was investigated in 21 patients with late-onset cerebellar ataxia (CA) or multiple system atrophy. The study included an initial investigation and a follow-up examination on average 25.3 months later (minimum 8, maximum 36). Patients were divided into four groups: (1) those with pure CA after a minimum course of 5 years; (2) those with pure CA with pathological neurophysiological findings at the last examination; (3) those who at the first examination clinically presented with pure CA, but at the last examination were seen to have developed a multisystem disorder; (4) those with multiple system atrophy (mostly olivopontocerebellar atrophy) presenting additional non-cerebellar signs of involvement. Conforming to a strict interpretation of pure CA, group 1 patients invariably exhibited normal neurophysiological findings at all examinations. All patients in group 4, except for 2 only at the first examination, showed pathological changes in at least one of the neurophysiological tests. The main conclusion of this paper is that individuals who according to clinical criteria were initially classified as having CA but finally developed a multisystem disorder already had pathological neurophysiological findings at the initial examination (group 3). The increasing frequency of pathology in the several neurophysiological tests together with the progression of the disease is obviously of prognostic significance. CT revealed cerebellar atrophy without apparent involvement of brain-stem structures in all patients with CA; the majority of patients with multiple system atrophy also had atrophy of the brain-stem, pointing to olivopontocerebellar atrophy.(ABSTRACT TRUNCATED AT 250 WORDS)
对21例迟发性小脑共济失调(CA)或多系统萎缩患者进行了神经生理学检查(脑干听觉诱发电位、眨眼反射、感觉、运动和视觉诱发电位)及CT随访。该研究包括一次初始检查以及平均25.3个月后的随访检查(最短8个月,最长36个月)。患者被分为四组:(1)病程至少5年的单纯CA患者;(2)上次检查时有病理神经生理学表现的单纯CA患者;(3)首次检查时临床诊断为单纯CA,但上次检查时已发展为多系统疾病的患者;(4)伴有其他非小脑受累体征的多系统萎缩患者(主要为橄榄脑桥小脑萎缩)。按照对单纯CA的严格定义,第1组患者在所有检查中神经生理学表现均正常。第4组所有患者,除2例仅在首次检查时正常外,至少一项神经生理学检查显示有病理改变。本文的主要结论是,根据临床标准最初被归类为CA,但最终发展为多系统疾病的个体在初次检查时已有病理神经生理学表现(第3组)。几种神经生理学检查中病理改变频率的增加以及疾病的进展显然具有预后意义。CT显示,所有CA患者均有小脑萎缩,脑干结构无明显受累;大多数多系统萎缩患者也有脑干萎缩,提示橄榄脑桥小脑萎缩。(摘要截断于250字)