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神经元蜡样脂褐质沉积症的细胞病理学。一项高尔基体电子显微镜研究。

The cellular pathology of neuronal ceroid-lipofuscinosis. A golgi-electronmicroscopic study.

作者信息

Williams R S, Lott I T, Ferrante R J, Caviness V S

出版信息

Arch Neurol. 1977 May;34(5):298-305. doi: 10.1001/archneur.1977.00500170052010.

Abstract

A cerebral biopsy specimen from a 4-year-old girl with a moderately advanced stage of the late infantile form of neuronal ceroid-lipofuscinosis was observed in routine cell and fiber stains and in Golgi and electronmicroscopic preparations. There was no evidence of neuronal degeneration or loss. Golgi impregnations identified a fusiform enlargement of proximal axon segments of most pyramidal neurons and some polymorphic neurons but not of other cortical neuronal classes. Typical curvilinear inclusions were found in all cells and appeared to be impacted within the dilated proximal axon segments of pyramidal neurons. The numbers of type II synapses on the axon hillock and dilated proximal axon segments of pyramidal neurons were much reduced, whereas type I synapses remained abundant in the neuropil.

摘要

对一名患有中度晚期婴儿型神经元蜡样脂褐质沉积症的4岁女孩的脑活检标本进行了常规细胞和纤维染色以及高尔基染色和电子显微镜检查。没有神经元变性或丢失的证据。高尔基染色显示大多数锥体神经元和一些多形神经元的近端轴突段呈梭形肿大,但其他皮质神经元类型未见此现象。在所有细胞中均发现典型的曲线形包涵体,且似乎聚集在锥体神经元扩张的近端轴突段内。锥体神经元轴丘和扩张的近端轴突段上的II型突触数量大大减少,而I型突触在神经毡中仍然丰富。

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