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神经源性疾病和多发性肌炎中肌纤维纵向分裂的发病机制。

Pathogenesis of longitudinal splitting of muscle fibres in neurogenic disorders and in polymyositis.

作者信息

Swash M, Schwartz M S, Sargeant M K

出版信息

Neuropathol Appl Neurobiol. 1978 Mar-Apr;4(2):99-115. doi: 10.1111/j.1365-2990.1978.tb00551.x.

Abstract

Longitudinal splitting of muscle fibres has been studied in the biopsies of eighteen patients with neurogenic disorders, and of twenty with polymyositis. In neurogenic disorders splitting predominantly affects hypertrophied fibres, and is probably due to mechanical overload induced by normal loads imposed on a weakened muscle. A similar phenomenon occurs in hypertrophied fibres in chronic polymyositis. However, in acute, or active polymyositis an appearance resembling fibre splitting can result from sequestration of necrotic segments within a fibre and also from regeneration occurring within intact sarcolemmal tubes after segmental sub-endomysial necrosis. These different processes, which can be distinguished by light and ultrastructural criteria, are important compensatory factors in neuromuscular disorders.

摘要

对18例神经源性疾病患者和20例多发性肌炎患者的活检组织进行了肌纤维纵向分裂的研究。在神经源性疾病中,分裂主要影响肥大的纤维,可能是由于施加在虚弱肌肉上的正常负荷引起的机械过载所致。慢性多发性肌炎的肥大纤维中也会出现类似现象。然而,在急性或活动性多发性肌炎中,纤维内坏死节段的隔离以及节段性肌内膜下坏死完整肌管内发生的再生都可导致类似纤维分裂的外观。这些可通过光镜和超微结构标准区分的不同过程,是神经肌肉疾病的重要代偿因素。

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