非典型肺炎-CoV-2 感染者格林-巴利综合征的临床和流行病学问题综述:扩展综合综述

Alexander Cordero-Campos, José Camones-Huerta, Leslie Condori Quispe, Susana Guzman Carrasco, Gustavo Quispe-Villegas, Karina Chin-Wu, Kenneth Vargas-Suarez, Hugo Umeres Cáceres, Martín Tipismana Barbarán
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摘要

自2019年以来,有报道称COVID-19患者出现了吉兰-巴雷综合征(GBS)。本综述探讨了这些患者的病理生理学、临床特征、实验室检查结果和影像学特征的解释机制:对2019年12月至2022年4月期间发表在NCBI和Scielo上的相关研究进行了文献检索:结果:共找到 90 篇文章,其中 53 篇被纳入本文。未发现说明 GBS 与 COVID19 相关性的研究。发现的具体临床表现为反射亢进(56.95%)、反射减弱(19.44%)、肌无力(65.28%)、步态障碍(12.5%)、感觉减退(26.39%)、麻痹(30.55%)和排尿障碍(6.94%)。脑脊液检查结果包括白蛋白-细胞学解离(66.67%),平均蛋白质水平为 140.23 mg/dL(标清:106.71)。部分病例在磁共振成像检查中发现颈部脑膜、脑干和颅神经增强。GBS的主要变异是急性炎症性脱髓鞘性多发性神经病(56.94%)。神经传导检查结果为无 F 波(61.54%)、远端运动潜伏期延长(80%)、运动振幅下降(93.1%)和运动传导速度下降(75%)。此外,主要受累的神经有胫神经(20.21%)、腓神经(24.47%)、正中神经(20.21%)和尺神经(18.09%)。最常见的颅神经改变是双侧面瘫(25%)和单侧面瘫(13.89%):结论:原发性 GBS 变异为急性炎症性脱髓鞘性多发性神经病。脑脊液分析显示白蛋白-细胞学分离是最常见的发现,核磁共振检查显示颅神经增强。另一个鉴别特征是自主系统投入较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A review of the clinical and epidemiological aspects of Guillain-Barré syndrome in patients infected with SARS-CoV-2: An Extended Comprehensive Review
Since 2019, cases of patients with COVID-19 who developed Guillain-Barré Syndrome (GBS) have been reported. This review explores mechanisms that explain pathophysiology, clinical features, laboratory findings, and imaging characteristics in these patients.Methodology: A bibliographic search was made of studies on the topic published in NCBI and Scielo, between December 2019 and April 2022.Results: Ninety articles were found, 53 of which were included in this article. No studies were found that explain an association between GBS and COVID19. Specific clinical manifestations found were areflexia (56.95%), hyporeflexia (19.44%), muscle weakness (65.28%), gait disturbance (12.5%), hypoesthesia (26.39%), paresthesia (30.55%), and micturition disturbance (6.94%). The CSF findings included albumin-cytological dissociation (66.67%), and an average protein level of 140.23 mg/dL (SD: 106.71). Some cases reported enhancement of the cervical leptomeningeal, brainstem and cranial nerves on magnetic resonance imaging tests. The predominant variant of GBS was acute inflammatory demyelinating polyneuropathy (56.94%). The findings in the nerve conduction studies were the absence of F waves (61.54%), increased distal motor latency (80%), decreased motor amplitude (93.1%), and decreased motor conduction velocity (75%). In addition, the nerves mainly involved were the tibial (20.21%), peroneal (24.47%), median (20.21%), and ulnar (18.09%). The most frequent alteration of cranial nerves was bilateral (25%) and unilateral (13.89%) facial palsy.Conclusion: The primary GBS variant was Acute Inflammatory Demyelinating Polyneuropathy. Cerebrospinal fluid analysis revealed albumin-cytological dissociation as the most common finding, and MRI tests showed cranial nerves enhancements. An additional differential feature was the lower commitment of the autonomous system.
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