Jedrzejowska H
Acta Neuropathol. 1977 Feb 28;37(2):119-25. doi: 10.1007/BF00692057.
Two sporadic cases of amyloid polyneuropathy with clinical features corresponding to the Portuguese type of this disease were studied. Histological examination of sural nerve demonstrated a marked loss of myelinated and unmyelinated fibres in the case 1 due to axonal degeneration, high content of fibers with segmental demyelination and the occurrence of several enlarged axons filled with the 10 nm filaments (so-called giant axons). In the case 2 there was total loss of unmyelinated axons and myelinated fibers were nearly completely lacking. In the development of changes in the myelinated fibers their direct compression by amyloid deposits seems to play an important role. It leads to the appearance of both axonal degeneration and segmental demyelination. The latter seems to be due to local compression and it may involved many fibers. In the light of observations reported by other authors the mechanism of changes developing in unmuelinated fibers is explained by the presence of changes in the cells of posterior root ganglia, however the question whether some abnormalities seen in unmyelinated axons could not be related to the pressure exerted by amyloid deposits directly to these fibers, remains open.
研究了两例散发性淀粉样多神经病病例,其临床特征与葡萄牙型该病相符。对腓肠神经的组织学检查显示,病例1中由于轴突变性,有髓和无髓纤维明显丧失,节段性脱髓鞘纤维含量高,且出现了几条充满10纳米细丝的增大轴突(所谓的巨大轴突)。病例2中无髓轴突完全丧失,有髓纤维几乎完全缺失。在有髓纤维变化的发展过程中,淀粉样沉积物对其直接压迫似乎起重要作用。这导致了轴突变性和节段性脱髓鞘的出现。后者似乎是由于局部压迫,可能涉及许多纤维。根据其他作者报道的观察结果,无髓纤维中变化的机制是由后根神经节细胞的变化来解释的,然而,无髓轴突中所见的一些异常是否与淀粉样沉积物直接对这些纤维施加的压力无关,这个问题仍然悬而未决。