首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >An autopsy case of incipient Pick's disease: Immunohistochemical profile of early-stage Pick body formation
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An autopsy case of incipient Pick's disease: Immunohistochemical profile of early-stage Pick body formation

机译:早期匹克氏病的尸检病例:早期匹克体形成的免疫组织化学特征

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There is little immunohistochemical information about the early stage of Pick body formation, due to the extremely limited opportunities of studying Pick's disease at the incipient or subclinical stage. We report a 62-year-old man without any clinical manifestations of Pick's disease, who died of B-cell lymphoma of the brainstem. Post mortem examination revealed many Pick bodies without obvious neuronal loss mainly in the left frontal and temporal lobes. Three brains of patients with typical Pick's disease (disease duration: 7, 11 and 16 years) were also examined. Pick bodies were immunopositive for phosphorylated tau and 3-repeat tau, and less consistently for p62 in both incipient and typical cases. In the incipient case, borderline positivity for ubiquitin was evident in only a few Pick bodies, whereas in the typical cases many Pick bodies showed obvious positivity for ubiquitin. These findings suggest that Pick bodies are rarely ubiquitinated in the early stage of Pick body formation.
机译:由于在初期或亚临床阶段研究Pick病的机会非常有限,因此关于Pick身体形成早期的免疫组织化学信息很少。我们报告了一名62岁的老人,没有任何Pick病的临床表现,他死于脑干B细胞淋巴瘤。验尸显示,许多匹克氏体没有明显的神经元丢失,主要在左额叶和颞叶。还检查了患有典型匹克氏病(疾病持续时间:7、11和16岁)的患者的三只大脑。截短体对磷酸化的tau和3重复tau免疫阳性,而在初期和典型情况下p62的免疫力均较弱。在初期情况下,泛素的临界阳性仅在少数匹克体中明显,而在典型情况下,许多匹克体对泛素显示出明显的正性。这些发现表明,匹克小体在匹克小体形成的早期很少被泛素化。

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