Desai J, Swash M
The Department of Neurology, The Royal London Hospital, London E1 1BB, UK.
J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):214-6. doi: 10.1136/jnnp.67.2.214.
Three patients with sporadic amyotrophic lateral sclerosis (ALS) presented with a history of backward falls. Impaired postural reflexes and retropulsion accompanied clinical features of ALS. Hypokinesia, decreased arm swing, and a positive glabellar tap were noted in two of these three patients. Cognitive impairment, tremor, axial rigidity, sphincter dysfunction, nuchal dystonia, dysautonomia, and oculomotor dysfunction were absent. Brain MRI disclosed bilateral T2 weighted hyperintensities in the internal capsule and globus pallidus in one patient. Necropsy studies performed late in the course of ALS have shown degeneration in extrapyramidal sites-for example, the globus pallidus, thalamus, and substantia nigra. Clinically, backward falls and retropulsion may occur early in ALS. This may reflect extrapyramidal involvement.
三名散发性肌萎缩侧索硬化症(ALS)患者有向后跌倒的病史。姿势反射受损和后冲现象伴随ALS的临床特征出现。这三名患者中有两名出现运动减少、摆臂减少和眉间轻叩试验阳性。未出现认知障碍、震颤、轴性强直、括约肌功能障碍、颈部肌张力障碍、自主神经功能障碍和动眼神经功能障碍。脑部MRI显示一名患者内囊和苍白球有双侧T2加权高信号。在ALS病程后期进行的尸检研究显示锥体外系部位出现变性,如苍白球、丘脑和黑质。临床上,向后跌倒和后冲现象可能在ALS早期出现。这可能反映了锥体外系受累。