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额叶型痴呆患者脑组织的病理改变特征:1例报告
引用本文:林世和,赵节绪,江新梅,宋晓南,蒋淑珍. 额叶型痴呆患者脑组织的病理改变特征:1例报告[J]. 中国组织工程研究与临床康复, 2005, 9(13): 215-217
作者姓名:林世和  赵节绪  江新梅  宋晓南  蒋淑珍
作者单位:吉林大学第一医院神经内科,吉林省长春市,130021
摘    要:背景额叶型痴呆患者脑组织的病理改变尚有争议,文章通过1例已死亡痴呆患者脑组织的病理研究,提出额叶型痴呆脑组织病理改变特征.目的拟证实一种非常见的伴有痴呆的神经系统变性疾病--额叶型痴呆.设计病例分析.单位吉林大学第一医院神经内科.方法对1例进行性痴呆患者死后3h进行脑部解剖检查,系列的组织染色及PrP,tau蛋白等免疫组织化学染色.主要观察指标①临床症状.②头部CT和脑电图检查结果.③脑部解剖检查结果.④免疫组织化学染色结果.结果①进行性神经、精神症状,病程为3年.②头部CT示双侧额叶灰质萎缩,脑电图呈阵发性全导联,长间歇期(>2 s)的高波幅慢波.③脑质量1 050 g,脑萎缩仅限于额叶,未累及颞叶.④额叶灰质从第2层开始神经细胞大量脱失伴明显胶质增生,而锥体细胞相对完好.Beilschowsky及Gallyas染法无异常发现.⑤神经细胞及胶质细胞内未发现任何包涵体.⑥PrP,tau蛋白免疫组织化学染色呈阴性反应.结论该病例为典型额叶型痴呆,今后在分析伴有痴呆的神经系统变性疾病时,应想到此类型痴呆.

关 键 词:痴呆  额叶萎缩  免疫组织化学

Pathological alterative characteristics of the brain tissue in patients with dementia of frontal lobe: one case report
LIN Shi-he,Zhao Jie-xu,JIANG Xin-mei,Song Xiao-nan,JIANG Shu-zhen. Pathological alterative characteristics of the brain tissue in patients with dementia of frontal lobe: one case report[J]. Journal of Clinical Rehabilitative Tissue Engineering Research, 2005, 9(13): 215-217
Authors:LIN Shi-he  Zhao Jie-xu  JIANG Xin-mei  Song Xiao-nan  JIANG Shu-zhen
Abstract:BACKGROUND: Pathological changes of the brain tissue in patients with dementia of frontal type(DFT) are still controversial. This paper brought forward the pathological alterative characteristics of brain tissue in DFT patients through one pathological case study of the brain tissue in one dead dementia patient.OBJECTIVE: To validate one uncommon neurodegenerative disease complicated with dementia, DFT.DESIGN: A case analysis.SETTING: Department of Neurology of the First Hospital of Jilin University METHODS: Brain anatomy, serials of histological staining and immunohistochemical staining for PrP, tau protein, etc. were performed after 3 hours since the death of one patient with progressive dementia.stainingfrontal lobes. EEG displayed a paroxysmal high-amplitude slow wave with and the brain atrophy was limited to frontal lobe and the temporal lobe loss of neurocyte companied with significant gliosis since the second layer; However, the pyramidal cell was relatively healthy. No abnormality was munohistochemical staining had negative reactions.CONCLUSION: This case was typical DFT. This type of dementia should be considered in future analysis of the neurodegenerative disease complicated with dementia.
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