Warcup Alice, Movio Guilherme, Dhar Saikat, Till Christopher
Medical Education, Lancaster Medical School, Lancaster, GBR.
Neurology, Royal Preston Hospital, Lancashire Teaching Hospitals NHS Foundation Trust, Lancashire, GBR.
Cureus. 2024 Jun 4;16(6):e61653. doi: 10.7759/cureus.61653. eCollection 2024 Jun.
A woman in her 60s initially presented with rapid-onset left-sided hemiparesis with later development of slurred speech and left-sided facial droop. Despite ruling out common causes, her condition rapidly progressed with the development of bilateral proximal weakness, ophthalmoplegia, ataxia, and pyramidal signs eventually leading to a cardiorespiratory arrest. Extensive investigations, including computerised tomography (CT), magnetic resonance imaging (MRI), and lumbar puncture (LP), were negative for infectious or vascular aetiologies. Nerve conduction studies (NCS) revealed severe peripheral nerve damage, and despite a provisional diagnosis of Guillain-Barré Syndrome (GBS), the clinical picture aligned more with Bickerstaff Brainstem Encephalitis (BBE) given the central nervous system (CNS) involvement, despite negative anti-GM1 and anti-GQ1b autoantibodies. Treatment involved ventilatory support, immunoglobulins, and steroids. This case report describes a rare and challenging presentation of BBE and reminds clinicians to have a systematic approach to a patient presenting with rapid onset neurological symptoms and that BBE is a clinical diagnosis.
一名60多岁的女性最初表现为急性发作的左侧偏瘫,随后出现言语不清和左侧面部下垂。尽管排除了常见病因,但她的病情迅速进展,出现双侧近端肌无力、眼肌麻痹、共济失调和锥体束征,最终导致心肺骤停。包括计算机断层扫描(CT)、磁共振成像(MRI)和腰椎穿刺(LP)在内的广泛检查未发现感染或血管病因。神经传导研究(NCS)显示严重的周围神经损伤,尽管初步诊断为吉兰-巴雷综合征(GBS),但鉴于中枢神经系统(CNS)受累,临床症状更符合比克斯特法夫脑干脑炎(BBE),尽管抗GM1和抗GQ1b自身抗体检测为阴性。治疗包括通气支持、免疫球蛋白和类固醇。本病例报告描述了BBE一种罕见且具有挑战性的表现,并提醒临床医生对出现急性神经系统症状的患者要有系统的诊疗方法,且BBE是一种临床诊断。