[Immune-mediated polyneuropathies].

IF 0.6 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Medicina-buenos Aires Pub Date : 2025-09-01
Silvia Cerezo, Jesica Expósito, Laura Carrera, Daniel Natera, Andrés Nascimento, Carlos Ortez
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引用次数: 0

Abstract

The Guillain-Barré syndrome (GBS) represents a group of immune-mediated peripheral polyneuropathies, which are the most common cause of acute flaccid paralysis in clinical practice. Its most prevalent form is acute inflammatory demyelinating polyneuropathy (AIDP), though multiple variants are also recognized, such as axonal neuropathies (AMAN, AMSAN) and MillerFisher syndrome. Diagnosis remains primarily clinical, supported by findings in cerebrospinal fluid analysis, neurophysiological studies, and, in certain cases, specific serology. Early detection is crucial to prevent potentially fatal complications such as respiratory failure or severe dysautonomia. This article provides an updated review of the diagnostic and therapeutic approaches to GBS, emphasizing its pathophysiology, clinical manifestations, first-line therapeutic strategies, and emerging variants treatable with targeted immunotherapy.

免疫介导性多神经病。
吉兰-巴罗综合征(GBS)是一组免疫介导的周围多神经病变,在临床实践中是急性弛缓性麻痹的最常见原因。其最常见的形式是急性炎症性脱髓鞘性多神经病变(AIDP),尽管也有多种变体,如轴突神经病(AMAN, AMSAN)和米勒-费舍尔综合征。诊断仍然主要是临床诊断,由脑脊液分析、神经生理学研究以及在某些情况下的特定血清学结果支持。早期发现对于预防潜在的致命并发症(如呼吸衰竭或严重的自主神经异常)至关重要。本文综述了GBS的最新诊断和治疗方法,重点介绍了GBS的病理生理、临床表现、一线治疗策略以及可通过靶向免疫治疗的新变体。
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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来源期刊
Medicina-buenos Aires
Medicina-buenos Aires 医学-医学:内科
CiteScore
1.30
自引率
12.50%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Information not localized
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