Carvalho J, Coimbra A, Andrade C
Brain. 1976 Mar;99(1):1-10. doi: 10.1093/brain/99.1.1.
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.
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。