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家族性淀粉样多神经病患者无症状子女的周围神经纤维变化

Peripheral nerve fibre changes in asymptomatic children of patients with familial amyloid polyneuropathy.

作者信息

Carvalho J, Coimbra A, Andrade C

出版信息

Brain. 1976 Mar;99(1):1-10. doi: 10.1093/brain/99.1.1.

Abstract

Sural nerve biopsies of 5 children of patients with familial amyloid polyneuropathy were studied by electronmicroscopy. The subjects were 14-17 years old and were in normal health. Neurological examination was negative. In none of the sural nerve specimens were there any amyloid deposits. In Case 4 no fine structural changes were detected. In the remaining 4 cases, there were frequent deposits of glycogen and clusters of multimembranous bodies in the Schwann-cell crescents of large myelinated fibres which presented infoldings of the myelin sheath, irregular myelin lamellation and a great number of Schmidt-Lanterman incisures. In one nerve fasciculus of Case 5 the myelin sheaths of some large myelinated fibres were extremely thickened; the axoplasm exhibited dilated vesicles and disordered microfilaments. These findings were taken as evidence of the occurrence of nerve fibre lesions at the pre-symptomatic stage of the disease, which seem to precede the appearance of amyloid deposition. The lesions affected primarily the Schwann cell and myelin sheath, and spared the unmyelinated fibres.

摘要

对5名家族性淀粉样多神经病患者的子女进行了腓肠神经活检,并进行了电子显微镜研究。受试者年龄在14至17岁之间,身体健康。神经学检查为阴性。在所有腓肠神经标本中均未发现淀粉样沉积物。病例4未检测到细微结构变化。在其余4例中,在有髓鞘折叠、髓鞘板层不规则和大量施密特-兰特尔曼切迹的大的有髓纤维的施万细胞半月体中,糖原沉积频繁,多膜体聚集。病例5的一个神经束中,一些大的有髓纤维的髓鞘极度增厚;轴浆显示出扩张的小泡和紊乱的微丝。这些发现被视为疾病症状前期神经纤维病变发生的证据,这些病变似乎先于淀粉样沉积物的出现。病变主要影响施万细胞和髓鞘,而未累及无髓纤维。

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