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[克劳-富卡塞综合征的病理学]

[Pathology of Crow-Fukase syndrome].

作者信息

Kanda Takashi

机构信息

Department of Neurology and Clinical Neuroscience, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamiogushi, Ube, Yamaguchi 755-8505, Japan.

出版信息

Brain Nerve. 2008 Jun;60(6):603-10.

Abstract

Although the exact mechanisms underlying peripheral neuropathy in Crow-Fukase syndrome (CFS), also known as POEMS syndrome, remain obscure, careful scrutiny of the pathological changes in the peripheral nervous system (PNS) and systemic organs by using biopsy and autopsy materials may provide useful information regarding the pathogenesis and future therapeutics of the syndrome. In this review, previous biopsy/autopsy studies on CFS were systematically reviewed and the details of the pathological changes in the PNS and vascular system were noted. Most biopsied nerves revealed the characteristics of axonal degeneration and demyelination together; however, the nerve roots obtained at autopsy showed massive demyelination with few axonal changes. This morphological discrepancy can be interpreted as primary demyelination in the proximal PNS and secondary axonal degeneration in the distal PNS. Another histological hallmark of the syndrome is edema in the endoneurial space. Changes in the endoneurial and epineurial microvessels, including hyperplasia of endothelial cells, were occasionally observed. Endoneurial edema and microvascular changes can be attributed to the high serum concentration of vascular endothelial growth factor in this disorder, and the derangement in endoneurial homeostasis due to impaired blood-nerve barrier can be considered a possible pathomechanism underlying peripheral neuropathy in the CFS.

摘要

尽管克劳-深濑综合征(CFS),也称为POEMS综合征,其周围神经病变的确切机制仍不清楚,但通过活检和尸检材料仔细研究周围神经系统(PNS)和全身器官的病理变化,可能会为该综合征的发病机制和未来治疗提供有用信息。在这篇综述中,我们系统回顾了先前关于CFS的活检/尸检研究,并记录了PNS和血管系统病理变化的细节。大多数活检神经同时显示出轴突变性和脱髓鞘的特征;然而,尸检获得的神经根显示出大量脱髓鞘,轴突变化很少。这种形态学差异可解释为近端PNS的原发性脱髓鞘和远端PNS的继发性轴突变性。该综合征的另一个组织学特征是神经内膜间隙水肿。偶尔观察到神经内膜和神经外膜微血管的变化,包括内皮细胞增生。神经内膜水肿和微血管变化可归因于该疾病中血管内皮生长因子的高血清浓度,并且由于血神经屏障受损导致的神经内膜内环境稳态紊乱可被认为是CFS中周围神经病变的一种可能病理机制。

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