Nodopathy: clinic, diagnosis, treatment. Clinical description

Al'bert R. Bulatov, I. Litvinenko, Nikolay V. Tsygan, Sergei N Bardakov, Aleksandra A. Boykova, Tatyana A. Kolesnik, Lyudmila S. Onishchenko
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Abstract

AIM: Evaluation of the significance and possibilities of laboratory-instrumental diagnostic methods in establishing the diagnosis and selection of targeted therapy in patients with nodopathies. MATERIALS AND METHODS: System analysis of data from foreign and domestic literature with the presentation of a clinical case. RESULTS: Polyneuropathies are classified as demyelinating or axonal based on electrophysiological studies. However, in 2015, in addition to axonal and demyelinating neuropathies, it was proposed to distinguish a separate pathophysiological group — nodopathies. The pathogenesis of nodopathies may differ depending on the type of ion channels involved in the process, but always leads to a loss of excitability of the axon membrane; in the nodal region the membrane becomes inexcitable. Such neuropathies are characterized by transient conduction blocks followed by the development of axonal degeneration. Typical examples of nodopathies are acute motor axonal neuropathy, as well as multifocal motor neuropathy. Current pathophysiological understanding of specialized nodal regions (nodes of Ranvier) and associated axoglial proteins is growing. Hypotheses have been put forward about their role in the pathogenesis of immune-mediated attack on the peripheral myelinated axon. Recently, high titers of antibodies directed against a number of key adhesion molecules have been identified in both acute and chronic inflammatory neuropathies. These facts add to the differences in differential diagnosis between axonal and demyelinating peripheral neuropathies. New disease classification schemes based on seropositivity, improved electrophysiological and ultrasound classification, and identification of putative underlying pathological targets and mechanisms are being rapidly developed. CONCLUSION: Using our clinical example, we demonstrated the capabilities of laboratory and instrumental diagnostic methods in establishing a diagnosis in a patient with one of the forms of nodopathies — multifocal motor neuropathy.
结节病:临床、诊断和治疗。临床描述
目的:评价实验室仪器诊断方法在确定结节病患者的诊断和选择靶向治疗方案中的意义和可能性。材料与方法:系统分析国内外文献资料,并结合1例临床病例。结果:基于电生理研究,多神经病变可分为脱髓鞘或轴突。然而,在2015年,除了轴突和脱髓鞘神经病变外,有人提出区分一个单独的病理生理组- nodopathies。结节病的发病机制可能因参与该过程的离子通道类型而异,但总是导致轴突膜兴奋性丧失;在结区,膜变得不可兴奋。这种神经病的特征是短暂的传导阻滞,随后是轴突变性的发展。结节病的典型例子是急性运动轴索神经病,以及多灶性运动神经病。目前对特化淋巴结区域(Ranvier淋巴结)和相关轴胶质蛋白的病理生理学理解正在增长。关于它们在免疫介导的外周髓鞘轴突攻击的发病机制中所起的作用,人们提出了假说。最近,针对一些关键黏附分子的高滴度抗体已经在急性和慢性炎症性神经病中被发现。这些事实增加了轴突和脱髓鞘周围神经病变鉴别诊断的差异。新的疾病分类方案基于血清阳性,改进的电生理和超声分类,并确定假定的潜在病理靶点和机制正在迅速发展。结论:通过我们的临床例子,我们展示了实验室和仪器诊断方法在诊断一种形式的结节病-多灶性运动神经病患者中的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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