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进行性核上性麻痹临床研究 被引量:6

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摘要 进行性核上性麻痹(progressive supranuclearpalsy,PSP)又称Steele-Richardson-Olszewski综合征。该病在美国适龄居民中患病率为1.39人/10万,但实际患病率可能远不止这一数字,因为很多病例在其发病很长一段时间后才明确诊断,而且有许多病例很可能至死亡时仍未明确诊断或误诊为其他疾病,尤其帕金森病。一、病理大体标本可见苍白球、黑质和脑干萎缩,第Ⅲ、Ⅳ脑室及侧脑室扩大;黑质和蓝斑脱色;Brodmann 4区中度萎缩。镜下特征性神经病理改变是基底节和脑干分布大量的神经纤维缠结(neurofibrillary tan-gles,NFT)和线型神经纤维网结构(neuropilthreads),同时伴神经元缺失、星形胶质细胞增生。典型病例NFT分布在苍白球、下丘脑核、纹状体、
出处 《中国临床神经科学》 1999年第1期58-61,共4页 Chinese Journal of Clinical Neurosciences
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  • 1P. Vermersh,A. Wattez,A. Delacourte,Y. Robitaille,L. Bernier,D. Gauvreau. Biochemical mapping of neurofibrillary degeneration in a case of progressive supranuclear palsy: evidence for general cortical involvement[J] 1994,Acta Neuropathologica(6):572~577

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  • 1侯静,陈彤,张晓红,吴卫平,王振福,郭瑞表.103例国人进行性核上性麻痹患者的临床特征[J].神经病学与神经康复学杂志,2010,7(3):135-141. 被引量:14
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