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重症肌无力中的神经源性肌肉萎缩

Neurogenic muscle atrophy in myasthenia gravis.

作者信息

Brownell B, Oppenheimer D R, Spalding J M

出版信息

J Neurol Neurosurg Psychiatry. 1972 Jun;35(3):311-22. doi: 10.1136/jnnp.35.3.311.

Abstract

Two cases of severe myasthenia gravis are described, with histological findings. Both cases showed severe neurogenic atrophy of the muscles of the tongue, with fatty pseudohypertrophy and a remarkable proliferation of terminal nerve fibres. Similar, but less severe, changes were present in other bulbar muscles. The findings are in keeping with the view that functional interruption at the neuromuscular junctions results first in failure to transmit the contractile impulse, and at a later stage in denervation atrophy. Terminal proliferation of axons is regarded as an attempt, on the part of motor fibres, to compensate for the breakdown of normal neuromuscular interaction.

摘要

本文描述了两例重症肌无力病例及其组织学检查结果。两例均显示舌肌严重神经源性萎缩,伴有脂肪性假肥大及终末神经纤维显著增生。其他延髓肌也有类似但程度较轻的改变。这些发现支持以下观点:神经肌肉接头处的功能中断首先导致收缩冲动传递失败,随后导致失神经萎缩。轴突终末增生被认为是运动纤维试图补偿正常神经肌肉相互作用破坏的一种尝试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1092/494071/a0445b653537/jnnpsyc00207-0028-a.jpg

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