Overview of symptoms, pathogenesis, diagnosis, treatment, and prognosis of various acquired polyneuropathies

Hyun-Jung Yu, S. Koh
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引用次数: 3

Abstract

Polyneuropathy means a lot of diseases affecting peripheral nerves showing roughly the same areas on both sides of the body, featuring weakness, numbness, and burning pain [1]. Pathogenesis causing polyneuropathy usually begins in the hands and feet and progresses to the arms and legs [1]. Sometimes it can involve other parts of the body such as the autonomic nervous system. Uncountable causes can induce acute or chronic polyneuropathy, so finding the original cause is most important for the treatment of polyneuropathy. Polyneuropathies are classified in different ways depending on cause, presentation, or classes of polyneuropathy (for example, the axon, the myelin sheath, or the cell body). Among these classifications, the classification based on classes of polyneuropathy can explain the pathogenesis and symptoms at the same time. Polyneuropathy in the axon is called distal axonopathy which is the result of interrupted function of the peripheral nerves and the most common response of neurons to metabolic or toxic disturbances, such as diabetes, kidney failure, connective tissue disease, deficiency syndrome, alcoholism, chemotherapy, and so on. People with distal axonopathy frequently present with sensorimotor disturbances. Disease in the myelin sheath is myelinopathy characterized with a loss of myelin or of the Schwann cells. This demyelination disturbs the conduction of action potentials through the axon of the nerve cells. Among various diseases causing myelinopathy, the most common one is acute inflammatory demyelinating polyneuropathy (AIDP). Damage of neurons in the peripheral nervous system results in neuronopathy. Neuronopathies can Corresponding Author: Seong-Ho Koh Department of Neurology, Hanyang University Guri Hospital, Hanyang University College of Medicine, 153 Gyeongchun-ro, Guri 11923, Korea Tel: +82-31-560-2267 Fax: +82-31-560-2267 E-mail: ksh213@hanyang.ac.kr
各种获得性多神经病变的症状、发病机制、诊断、治疗和预后概述
多神经病变是指影响周围神经的多种疾病,表现在身体两侧大致相同的区域,以无力、麻木、灼痛为特征[1]。多神经病变的发病机制通常始于手足,并向手臂和腿部发展[1]。有时它会涉及到身体的其他部位,比如自主神经系统。许多原因都可能诱发急性或慢性多发性神经病变,因此找到病因对于多发性神经病变的治疗至关重要。根据病因、表现或多神经病变的种类(如轴突、髓鞘或细胞体),多神经病变有不同的分类。在这些分类中,基于多神经病变的分类可以同时解释发病机制和症状。轴突的多神经病变被称为远端轴索病,它是周围神经功能中断的结果,是神经元对代谢或毒性紊乱的最常见反应,如糖尿病、肾衰竭、结缔组织疾病、缺乏综合征、酒精中毒、化疗等。远端轴突病患者常表现为感觉运动障碍。髓鞘疾病是一种髓鞘病,其特征是髓鞘或雪旺细胞的丧失。这种脱髓鞘干扰了神经细胞轴突的动作电位传导。在引起髓鞘病的各种疾病中,最常见的是急性炎症性脱髓鞘性多神经病变(AIDP)。周围神经系统神经元的损伤导致神经病变。通讯作者:kseung - ho Koh汉阳大学九里医院神经内科,汉阳大学医学院,京春路153号,九里11923,韩国电话:+82-31-560-2267传真:+82-31-560-2267 E-mail: ksh213@hanyang.ac.kr
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