THE CLINICAL AND PATHOLOGICAL SPECTRUM OF STEELE-RICHARDSON-OLSZEWSKI SYNDROME (PROGRESSIVE SUPRANUCLEAR PALSY) - A REAPPRAISAL

被引：236
作者：
DANIEL, SE
DEBRUIN, VMS
LEES, AJ
机构：
[1] INST NEUROL,DEPT NEUROPATHOL,LONDON WC1N 1PJ,ENGLAND
[2] UNIV LONDON,INST NEUROL,DEPT CLIN NEUROL,LONDON,ENGLAND
[3] ESCOLA PAULISTA MED,DEPT PSICOBIOL,SAO PAULO,BRAZIL
来源：
BRAIN | 1995年 / 118卷
关键词：
STEELE-RICHARDSON-OLSZEWSKI SYNDROME; SUPRANUCLEAR GAZE PALSY; CLASSIFICATION; CLINICOPATHOLOGICAL CORRELATION;
D O I：
10.1093/brain/118.3.759
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Seventeen patients with a progressive bradykinetic syndrome and post-mortem findings of neurofibrillary degeneration in cerebral cortex, subcortical nuclei and brainstem were studied. Seven fulfilled currently accepted clinical diagnostic criteria for Steele-Richardson-Olszewski syndrome, whereas the remainder who lacked supranuclear gaze palsy had alternative clinical diagnoses (idiopathic Parkinson's disease, six cases; cerebrovascular disease, two cases; Parkinson's syndrome, one case; Alzheimer's disease, one case). The clinical and pathological findings of the two groups were compared in an attempt to better define the spectrum of Steele-Richardson-Olszewski disease.
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页码：759 / 770
页数：12
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共 87 条
[1]  
Abe H., Yagishita S., Amano N., Bise K., Ultrastructural and immunohistochemical study of ‘astrocytic tangles’ (ACT) in patients with progressive supranuclear palsy, Clin Neuropathol, 5, (1993)
[2]  
Agid Y., Javoy-Agid F., Ruberg M., Pillon B., Dubois B., Duyckaerts C., Et al., Progressive supranuclear palsy: Anatomoclinical and biochemical considerations, Adv Neurol, 4, pp. 191-206, (1987)
[3]  
Akashi T., Arima K., Maruyama N., O S., Inose T., Severe cerebral atrophy in progressive supranuclear palsy: A case report, Clin Neuropathol, 8, pp. 195-199, (1989)
[4]  
Alajouanine T., Delafontaine P., Lacan J., Duregard Par Hypertonie F., Prédominant dans le sens vertical, avec conservation des mouvements automatico-réflexes, aspect spéciale de syndrome de Parinaudpar hypertonie associée à un syndrome extrapyramidal avec troubles pseudobulbaires, Rev Neurol (Paris), 2, pp. 410-418, (1926)
[5]  
Albert M.L., Feldman R.G., Willis A.L., The ‘subcortical dementia’ of progressivesupranuclear palsy, J Neurol Neurosurg Pychiatry, 3, pp. 121-130, (1974)
[6]  
Arima K., Murayama S., Oyanagi S., Akashi T., Inose T., Presenile dementia with progressive supranuclear palsy tangles and Pick bodies: An unusual degenerative disorder involving the cerebral cortex, cerebral nuclei, and brain stem nuclei, Acta Neuropathol (Berl), 8, pp. 128-134, (1992)
[7]  
Bancher C., Lassmann H., Budka H., Grundke-Iqbal I., Iqbal K., Wiche G., Et al., Neurofibrillary tangles in Alzheimer’s disease and progressive supranuclear palsy: Antigenic similarities and differences, Acta Neuropathol (Berl), 7, pp. 39-46, (1987)
[8]  
Behrman S., Carroll J.D., Janota I., Matthews W.B., Progressive supranuclear palsy. Clinico-pathological study of four cases, Brain, 9, pp. 663-678, (1969)
[9]  
Braak H., Braak E., Cortical and subcortical argyrophilic grains characterize a disease associated with adult onset dementia, Neuropathol Appl Neurobiol, 1, pp. 13-26, (1989)
[10]  
Braak H., Braak E., The human entorhinal cortex: Normal morphology and lamina-specific pathology in various diseases. [Review], Neurosci Res, 1, pp. 6-31, (1992)
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