Suppr超能文献

伴有肿胀性染色质溶解神经元的皮质变性:其与皮克病的关系。

Cortical degeneration with swollen chromatolytic neurons: its relationship to Pick's disease.

作者信息

Clark A W, Manz H J, White C L, Lehmann J, Miller D, Coyle J T

出版信息

J Neuropathol Exp Neurol. 1986 May;45(3):268-84. doi: 10.1097/00005072-198605000-00011.

Abstract

We report two cases of dementia in which cortical degeneration with widespread swollen chromatolytic neurons (SCN) was the dominant pathologic feature. Each patient had received the diagnosis of Alzheimer's disease on the basis of clinical findings. There was no deficit of cortical choline acetyltransferase activity, assayed in one case, or lesions of the nucleus basalis of Meynert. The brains had moderate to marked frontal atrophy. Comparison of SCN with several other cerebral degenerative disorders indicates a similarity with certain features of the transmissible spongiform encephalopathies and with corticodentatonigral degeneration. The pathologic features of our cases are those of a number of other cases reported as "Pick's disease," and may represent an earlier stage in the pathogenetic process than the severe, sharply circumscribed atrophy with "nonspecific" cell loss and gliosis as the only microscopic residuals. Our findings re-emphasize the need to search for pathogenetically distinct subgroups which have been wholly or partially subsumed into the concept of Pick's disease.

摘要

我们报告了两例痴呆病例,其中以广泛肿胀的染色质溶解神经元(SCN)的皮质变性为主要病理特征。根据临床发现,每位患者均被诊断为阿尔茨海默病。在其中一例中检测到皮质胆碱乙酰转移酶活性无缺陷,且无迈内特基底核病变。大脑有中度至明显的额叶萎缩。将SCN与其他几种脑退行性疾病进行比较表明,它与可传播性海绵状脑病的某些特征以及皮质齿状核黑质变性相似。我们病例的病理特征与其他一些被报告为“皮克病”的病例相同,并且可能代表了发病过程中比严重的、界限分明的萎缩更早的阶段,后者以“非特异性”细胞丢失和胶质增生作为唯一的微观残留。我们的发现再次强调了寻找在发病机制上不同的亚组的必要性,这些亚组已全部或部分被纳入皮克病的概念中。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验