Suppr超能文献

复发性格林-巴利综合征与急性起病慢性炎症性多发性神经病的鉴别:文献综述

Differentiating recurrent Guillain-Barre syndrome and acute-onset chronic inflammatory polyneuropathy: literature review.

作者信息

Inan Berin, Bekircan-Kurt Can Ebru, Demirci Mehmet, Erdem-Ozdamar Sevim, Tan Ersin

机构信息

Department of Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Department of Neurology, Gulhane Faculty of Medicine, University of Health Sciences, Ankara, Turkey.

出版信息

Acta Neurol Belg. 2024 Oct;124(5):1467-1475. doi: 10.1007/s13760-024-02557-2. Epub 2024 Apr 25.

Abstract

Guillain-Barre syndrome (GBS) is an acute-onset immune-mediated polyneuropathy characterized by ascending symmetrical muscle weakness, diminished reflexes, and sensory symptoms. While GBS typically follows a monophasic course, some patients experience treatment-related fluctuations or recurrences, posing diagnostic challenges in distinguishing GBS from acute-onset chronic inflammatory polyneuropathy (A-CIDP). A-CIDP, may present acutely, simulating GBS, with a nadir in less than 8 weeks, subsequently evolving into a chronic or relapsing course. The distinction between recurrent GBS and A-CIDP is crucial, as A-CIDP necessitates long-term immunosuppression. A PubMed search was conducted using the search terms 'recurrent Guillain Barre syndrome' and 'acute onset CIDP' focusing on studies in the English language, published between January 1, 2004 and April 30, 2023. Overlapping clinical features, particularly in the early stages, complicate differentiation between recurrent GBS and CIDP. Electrophysiological studies, ultrasonography, and immunological markers have been explored for discrimination; however, definitive criteria for differentiation remain elusive. Recent follow-up studies have further blurred the boundaries between recurrent GBS and A-CIDP, suggesting the persistence of underlying immune processes even in GBS patients without clinical deterioration. This emphasizes the necessity of reevaluating diagnostic criteria and treatment strategies. In conclusion, distinguishing recurrent GBS from A-CIDP remains an ongoing challenge. Existing evidence questions the categorization of recurrent GBS as a distinct entity, challenging its very existence. Continued research is necessary to refine diagnostic criteria and deepen our understanding of these conditions, ultimately advancing patient care. This review delves into the intricacies of recurrent GBS and A-CIDP differentiation and highlights the need for a reevaluation of the recurrent GBS concept.

摘要

吉兰 - 巴雷综合征(GBS)是一种急性起病的免疫介导性多发性神经病,其特征为进行性对称性肌无力、反射减弱和感觉症状。虽然GBS通常呈单相病程,但一些患者会出现与治疗相关的波动或复发,这在鉴别GBS与急性起病的慢性炎症性多发性神经病(A - CIDP)时带来了诊断挑战。A - CIDP可能急性起病,类似于GBS,在8周内达到最低点,随后发展为慢性或复发病程。复发性GBS与A - CIDP的区分至关重要,因为A - CIDP需要长期免疫抑制。使用搜索词“复发性吉兰 - 巴雷综合征”和“急性起病的CIDP”在PubMed上进行了搜索,重点关注2004年1月1日至2023年4月30日期间发表的英文研究。重叠的临床特征,尤其是在早期阶段,使复发性GBS和CIDP的鉴别变得复杂。人们已经探索了电生理研究、超声检查和免疫标志物用于鉴别;然而,明确的鉴别标准仍然难以捉摸。最近的随访研究进一步模糊了复发性GBS和A - CIDP之间的界限,表明即使在没有临床恶化的GBS患者中,潜在的免疫过程也持续存在。这强调了重新评估诊断标准和治疗策略的必要性。总之,区分复发性GBS和A - CIDP仍然是一个持续的挑战。现有证据对复发性GBS作为一个独特实体的分类提出了质疑,挑战了它的存在。持续的研究对于完善诊断标准和加深我们对这些疾病的理解是必要的,最终推动患者护理的进步。这篇综述深入探讨了复发性GBS和A - CIDP鉴别诊断的复杂性,并强调了重新评估复发性GBS概念的必要性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验