Department of Neurology, Hospital Dierdorf-Selters, Selters, Germany.
J Peripher Nerv Syst. 2020 Jun;25(2):204-207. doi: 10.1111/jns.12382. Epub 2020 May 26.
Acute demyelinating inflammatory polyneuropathy (AIDP) is the most common type of Guillain-Barré syndrome (GBS) in Europe, following several viral and bacterial infections. Data on AIDP-patients associated with SARS-CoV-2 (coronavirus-2) infection are scarce. We describe the case of a 54-years-old Caucasian female patient with typical clinical and electrophysiological manifestations of AIDP, who was reported positive with PCR for SARS-CoV-2, 3 weeks prior to onset of the neurological symptoms. She did not experience a preceding fever or respiratory symptoms, but a transient loss of smell and taste. At the admission to our neurological department, a progressive proximally pronounced paraparesis, areflexia, and sensory loss with tingling of all extremities were found, which began 10 days before. The modified Erasmus Giullain-Barré Syndrome outcome score (mEGOS) was 3/9 at admission and 1/12 at day 7 of hospitalization. The electrophysiological assessment proved a segmental demyelinating polyneuropathy and cerebrospinal fluid examination showed an albuminocytologic dissociation. The neurological symptoms improved significantly during treatment with immunoglobulins. Our case draws attention to the occurrence of GBS also in patients with COVID-19 (coronavirus disease 2019), who did not experience respiratory or general symptoms. It emphasizes that SARS-CoV-2 induces immunological processes, regardless from the lack of prodromic symptoms. However, it is likely that there is a connection between the severity of the respiratory syndrome and further neurological consequences.
急性炎症性脱髓鞘性多发性神经病(AIDP)是欧洲最常见的吉兰-巴雷综合征(GBS)类型,常继发于多种病毒和细菌感染。关于与 SARS-CoV-2(冠状病毒-2)感染相关的 AIDP 患者的数据很少。我们描述了一例 54 岁的高加索女性患者,其具有 AIDP 的典型临床和电生理表现,在神经系统症状出现前 3 周,PCR 检测 SARS-CoV-2 呈阳性。她没有发热或呼吸道症状,但有短暂的嗅觉和味觉丧失。在入住我们神经内科时,发现她存在进行性近端显著的四肢无力、反射消失和四肢刺痛感,这些症状在 10 天前开始出现。入院时改良的 Erasmus 吉兰-巴雷综合征结局评分(mEGOS)为 3/9,住院第 7 天为 1/12。电生理评估证实为节段性脱髓鞘多发性神经病,脑脊液检查显示蛋白细胞分离。免疫球蛋白治疗后,神经系统症状显著改善。我们的病例提请注意 COVID-19(2019 年冠状病毒病)患者也会发生 GBS,且这些患者没有呼吸道或全身症状。这强调了 SARS-CoV-2 会引起免疫过程,即使没有前驱症状。然而,呼吸综合征的严重程度与进一步的神经后果之间可能存在联系。