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病例报告:酷似中风的早发型吉兰-巴雷综合征

Case Report: Early-Onset Guillain-Barre Syndrome Mimicking Stroke.

作者信息

Sun Jing, Gao Yu, Chi Lumei, Cao Qingyang, Ning Zhijie, Nan Guangxian

机构信息

Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, China.

出版信息

Front Neurol. 2021 Feb 19;12:525699. doi: 10.3389/fneur.2021.525699. eCollection 2021.

Abstract

Guillain-Barre syndrome (GBS) is an acute immune-mediated inflammatory demyelinating polyneuropathy characterized by symmetrical limb weakness and areflexia. GBS can have different clinical manifestations; hence, the initial symptoms are also varied. Here, we describe a rare case of GBS presenting as hemiparesis and cranial nerve palsy, which mimic brainstem stroke. A 53-year-old man was admitted to the hospital with a 3-h history of left-arm weakness, glossolalia, and right eyelid droop. After admission, his condition suddenly worsened, with quadriplegia, bilateral peripheral facial palsy, bilateral ophthalmoplegia, and other neurological symptoms. Based on the findings from a neurological examination, MRI, cerebrospinal fluid analysis, and nerve conduction study, a diagnosis of GBS was made. He received intravenous immunoglobulin (0.4 kg/day) for 5 days. After 20 days of systematic therapy, his dysphagia, dyspnea, facial paralysis, ocular movement disorder, and leg weakness recovered almost completely, but his arms were still moderately impaired, with a power of 4/5. Fortunately, the patient recovered well without any sequelae after 2 years of follow-up. In patients with an atypical presentation, the diagnosis of GBS is often delayed. With this case report, we intend to highlight the fact that some symptoms mimicking stroke may be a feature of GBS at onset; close observation and timely diagnosis are crucial for clinicians. Neuroimaging is a valuable diagnostic tool in differentiating stroke from GBS.

摘要

吉兰-巴雷综合征(GBS)是一种急性免疫介导的炎性脱髓鞘性多发性神经病,其特征为对称性肢体无力和腱反射消失。GBS可有不同的临床表现;因此,初始症状也各不相同。在此,我们描述一例罕见的以偏瘫和脑神经麻痹为表现的GBS病例,其症状类似脑干卒中。一名53岁男性因左臂无力、言语不清和右眼睑下垂3小时入院。入院后,他的病情突然恶化,出现四肢瘫痪、双侧周围性面瘫、双侧眼肌麻痹及其他神经症状。根据神经检查、磁共振成像(MRI)、脑脊液分析及神经传导研究结果,诊断为GBS。他接受了静脉注射免疫球蛋白(0.4kg/天)治疗5天。经过20天的系统治疗,他的吞咽困难、呼吸困难、面瘫、眼球运动障碍及腿部无力几乎完全恢复,但双臂仍有中度功能障碍,肌力为4/5。幸运的是,经过2年随访,患者恢复良好,无任何后遗症。对于表现不典型的患者,GBS的诊断往往会延迟。通过本病例报告,我们旨在强调一些类似卒中的症状可能是GBS起病时的特征这一事实;密切观察和及时诊断对临床医生至关重要。神经影像学是鉴别卒中和GBS的一项有价值的诊断工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e565/7933233/bf7d9d97f20b/fneur-12-525699-g0001.jpg

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