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一例冯·埃科诺莫型脑炎后帕金森综合征的尸检病例:关于神经原纤维缠结和星形细胞缠结的一些新观察

An autopsy case of postencephalitic parkinsonism of von Economo type: some new observations concerning neurofibrillary tangles and astrocytic tangles.

作者信息

Haraguchi T, Ishizu H, Terada S, Takehisa Y, Tanabe Y, Nishinaka T, Kawai K, Kuroda S, Komoto Y, Namba M

机构信息

Department of Neuropsychiatry, Okayama University Medical School, Japan.

出版信息

Neuropathology. 2000 Jun;20(2):143-8. doi: 10.1046/j.1440-1789.2000.00287.x.

Abstract

An autopsied case of postencephalitic parkinsonism of von Economo type with a 71-year duration is reported. Several cases of postencephalitic parkinsonism of von Economo type have been reported in Japan but this is the first reported case from western Japan. The patient was a Japanese man who was 74 years of age at the time of death. He developed encephalitis of unknown etiology at the age of 3 years. The first symptom was antisocial behavior, which developed at 30 years of age. At the age of 40 years, the patient showed progressive parkinsonism. Neuropathological findings disclosed marked neuronal loss with gliosis in the substantia nigra, locus ceruleus, and raphe nuclei, as well as the appearance of neurofibrillary tangles in the aforementioned areas. There were also widespread tuft-shaped astrocytes (Tu-SA) in the central nervous system, including the thalamus. Tuft-shaped astrocytes are considered to represent non-reactive astrocytes because the distributions of neurofibrillary tangles (NFT) and Tu-SA are clearly different. Therefore, the primary astrocytic lesions in postencephalitic parkinsonism of von Economo type may be more widespread. Ultrastructurally, the Tu-SA consisted of straight filaments, 15 nm in width, which formed tight bundles. Ultrastructurally, NFF in this case revealed paired helical filaments but straight filaments, 15 nm in width, which were also found in the neurons of the substantia nigra.

摘要

报告了一例病程长达71年的冯·埃科诺莫型脑炎后帕金森综合征尸检病例。日本已报告了几例冯·埃科诺莫型脑炎后帕金森综合征病例,但这是日本西部首例报告病例。患者为一名日本男性,死亡时74岁。他3岁时患了病因不明的脑炎。最初症状是反社会行为,30岁时出现。40岁时,患者出现进行性帕金森综合征。神经病理学检查发现黑质、蓝斑和中缝核有明显的神经元丢失和胶质增生,上述区域还出现神经原纤维缠结。中枢神经系统,包括丘脑,也有广泛的簇状星形胶质细胞(Tu-SA)。簇状星形胶质细胞被认为代表非反应性星形胶质细胞,因为神经原纤维缠结(NFT)和Tu-SA的分布明显不同。因此,冯·埃科诺莫型脑炎后帕金森综合征的原发性星形细胞病变可能更广泛。超微结构上,Tu-SA由宽度为15nm的直丝组成,这些直丝形成紧密束状。超微结构上,该病例中的神经原纤维缠结显示为双螺旋丝,但在黑质神经元中也发现了宽度为15nm的直丝。

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