Khedr Eman M, Shoyb Ahmed, Mohamed Khaled O, Karim Ahmed A, Saber Mostafa
Department of Neurology and Psychiatry, Assiut University, Asyut, Egypt.
Department of Neuropsychiatry, Aswan University, Aswan, Egypt.
Front Neurol. 2021 Jun 22;12:678136. doi: 10.3389/fneur.2021.678136. eCollection 2021.
Guillain-Barré syndrome (GBS) is a potentially fatal, immune-mediated disease of the peripheral nervous system that is usually triggered by infection. Only a small number of cases of GBS associated with COVID-19 infection have been published. We report here five patients with GBS admitted to the Neurology, Psychiatry, and Neurosurgery Hospital, Assiut University/Egypt from July 1 to November 20, 2020. Three of the five patients were positive for SARS-CoV-2 following polymerase chain reaction (PCR) of nasopharyngeal swabs on day of admission and another one had a high level of IgM and IgG; all had bilateral ground-glass opacities with consolidation on CT chest scan (GGO) and lymphopenia. All patients presented with two or more of the following: fever, cough, malaise, vomiting, and diarrhea with variable duration. However, there were some peculiarities in the clinical presentation. First, there were only 3 to 14 days between the onset of COVID-19 symptoms and the first symptoms of GBS, which developed into flaccid areflexic quadriplegia with glove and stocking hypoesthesia. The second peculiarity was that three of the cases had cranial nerve involvement, suggesting that there may be a high incidence of cranial involvement in SARS-CoV-2-associated GBS. Other peculiarities occurred. Case 2 presented with a cerebellar hemorrhage before symptoms of COVID-19 and had a cardiac attack with elevated cardiac enzymes following onset of GBS symptoms. Case 5 was also unusual in that the onset began with bilateral facial palsy, which preceded the sensory and motor manifestations of GBS (descending course). Neurophysiological studies showed evidence of sensorimotor demyelinating polyradiculoneuropathy, suggesting acute inflammatory polyneuropathy (AIDP) in all patients. Three patients received plasmapheresis. All of them had either full recovery or partial recovery. Possible pathophysiological links between GBS and COVID-19 are discussed.
吉兰 - 巴雷综合征(GBS)是一种潜在致命的、由免疫介导的周围神经系统疾病,通常由感染引发。仅有少数与新型冠状病毒肺炎(COVID - 19)感染相关的GBS病例被报道。我们在此报告2020年7月1日至11月20日期间入住埃及阿斯尤特大学神经病学、精神病学和神经外科学院医院的5例GBS患者。5例患者中有3例在入院当天经鼻咽拭子聚合酶链反应(PCR)检测显示新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)呈阳性,另一例IgM和IgG水平较高;所有患者胸部CT扫描均显示双侧磨玻璃影伴实变(GGO)及淋巴细胞减少。所有患者均出现以下两种或更多症状:发热、咳嗽、不适、呕吐和腹泻,持续时间各异。然而,临床表现存在一些特殊之处。首先,COVID - 19症状出现至GBS首发症状之间仅间隔3至14天,随后发展为弛缓性无反射四肢瘫,并伴有手套袜套样感觉减退。第二个特殊之处在于3例患者出现颅神经受累,提示SARS-CoV-2相关GBS中颅神经受累发生率可能较高。还出现了其他特殊情况。病例2在COVID - 19症状出现前出现小脑出血,在GBS症状出现后发生心肌梗死且心肌酶升高。病例5也不寻常,其起病始于双侧面神经麻痹,先于GBS的感觉和运动表现(下行病程)。神经生理学研究显示所有患者均有感觉运动性脱髓鞘性多发性神经根神经病的证据,提示为急性炎症性多发性神经病(AIDP)。3例患者接受了血浆置换。所有患者均实现了完全康复或部分康复。本文还讨论了GBS与COVID - 19之间可能的病理生理联系。