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慢性复发性多神经炎

Chronic relapsing polyneuritis.

作者信息

Prineas J W, McLeod J G

出版信息

J Neurol Sci. 1976 Apr;27(4):427-58. doi: 10.1016/0022-510x(76)90213-6.

Abstract

Clinical, electrophysiological and pathological findings in 23 patients with subacute and relapsing idiopathic demyelinating polyneuropathies are described. In 17 patients with relapsing polyneuropathy, the neurological illness was unaccompanied by any systemic disturbances. The term preferred for the neuropathy in this group of patients is chronic relapsing polyneuritis. The findings in this group suggest that the common form of this syndrome is due to a single disease entity. Chronic relapsing polyneuritis differs from acute idiopathic polyneuritis chiefly in regard to the rate of evolution and the severity of the initial episode of polyneuropathy. If these two polyneuropathies have the same pathogenesis, the factor which determines whether the disease is acute and self-limiting or chronically relapsing is often present at the time of onset of the disease. The relationship of chronic relapsing polyneuritis to relapsing hypertrophic polyneuropathy and progressive hypertrophic polyneuropathy is also discussed and it is concluded that these diseases may constitute a spectrum of pathogenetically related disorders. In chronic relapsing polyneuritis, as in other demyelinating polyneuropathies, a marked segmental reduction in axon diameter accompanies demyelination. This corresponds to a more than 50% reduction in the volume of the affected region of the axon and it is associated with increased packing of axoplasmic organelles and wrinkling of the axolemma. It is suggested that in the normal myelinated nerve fibre, the Schwann cell and myelin sheath maintain fluid locally within the axon.

摘要

本文描述了23例亚急性和复发性特发性脱髓鞘性多发性神经病患者的临床、电生理和病理表现。在17例复发性多发性神经病患者中,神经系统疾病未伴有任何全身紊乱。该组患者中这种神经病的首选术语是慢性复发性多神经炎。该组的研究结果表明,这种综合征的常见形式是由单一疾病实体引起的。慢性复发性多神经炎与急性特发性多神经炎的主要区别在于疾病进展速度和多发性神经病初始发作的严重程度。如果这两种多发性神经病具有相同的发病机制,那么决定疾病是急性自限性还是慢性复发性的因素通常在疾病发作时就已存在。本文还讨论了慢性复发性多神经炎与复发性肥大性多发性神经病和进行性肥大性多发性神经病的关系,并得出结论,这些疾病可能构成一系列发病机制相关的疾病。在慢性复发性多神经炎中,与其他脱髓鞘性多发性神经病一样,脱髓鞘伴随着轴突直径的明显节段性减小。这相当于轴突受累区域体积减少超过50%,并且与轴浆细胞器的堆积增加和轴膜起皱有关。有人提出,在正常有髓神经纤维中,施万细胞和髓鞘在轴突内局部维持液体状态。

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