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晚期婴儿型、青少年型及晚发型异染性脑白质营养不良周围神经异常的超微结构比较观察

Comparative ultrastructural observations on peripheral nerve abnormalities in the late infantile, juvenile and late onset forms of metachromatic leukodystrophy.

作者信息

Thomas P K, King R H, Kocen R S, Brett E M

出版信息

Acta Neuropathol. 1977 Aug 31;39(3):237-45. doi: 10.1007/BF00691703.

Abstract

The ultrastructural findings in nerve biopsies from two cases of late onset metachromatic leukodystrophy were compared with those in cases of late infantile and juvenile onset. Hypertrophic changes and regenerating clusters were more evident in the late onset cases, in which macrophages were less frequent, presumably reflecting the chronicity of the disorder in this form. Inclusions within Schwann cells and endoneurial macrophages were similar in all four cases. Myelin figures, in which the periodicity of major dense lines was 8 nm, were present in Schwann cells associated with myelinated axons. The electron lucent zones between the major dense lines were bisected by lines of lesser electron density. These inclusions were probably related to myelin breakdown. All other inclusions displayed a periodicity of 5.8 nm and consisted of zebra bodies, vacuoles containing irregularly orientated lamellar material and stacks of flattened discs. These inclusions represented the metachromatic sulphatide deposits. Occasional inclusion bodies were observed within axons.

摘要

对两例晚发型异染性脑白质营养不良患者神经活检的超微结构结果与晚婴型和青少年型患者的结果进行了比较。肥大性改变和再生簇在晚发型病例中更为明显,其中巨噬细胞较少见,这可能反映了该型疾病的慢性病程。在所有四例病例中,施万细胞和神经内膜巨噬细胞内的包涵体相似。在与有髓轴突相关的施万细胞中存在髓鞘结构,其主要致密线的周期为8nm。主要致密线之间的电子透明区被电子密度较低的线一分为二。这些包涵体可能与髓鞘破坏有关。所有其他包涵体的周期为5.8nm,由斑马体、含有不规则排列的层状物质的空泡和平坦盘状堆叠组成。这些包涵体代表异染性硫脂沉积。偶尔在轴突内观察到包涵体。

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