Facial Diplegia Guillain-Barre Syndrome Variant Initially Presenting as a Stroke Mimic: Evolution from Unilateral Central-Appearing Facial Weakness to Bilateral Facial Palsy - A Case Report.

IF 0.4 Q4 CLINICAL NEUROLOGY
Case Reports in Neurology Pub Date : 2026-07-27 eCollection Date: 2026-01-01 DOI:10.1159/000553626
Fadel Alqatati, Rowan Mesilhy, Mohammad Ghabashneh, Kholoud Riyad Jaber, Noora Al-Abdulla, Amin S Sanosi, Shibu Kandalam Parampil T
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Abstract

Introduction: Facial diplegia is an uncommon regional variant of Guillain-Barre syndrome (GBS). It may initially resemble acute cerebrovascular disease when facial weakness appears unilateral or central in pattern.

Case presentation: A 48-year-old Sri Lankan man with untreated hypertension, obesity, and newly recognized diabetes presented approximately 18 h after onset of slurred speech and persistent left facial weakness. Initial examination suggested a left central facial palsy, although incomplete left eye closure was also present. Non-contrast computed tomography and same-day brain magnetic resonance imaging with angiography, performed approximately 25 h after symptom onset, showed no acute infarction, hemorrhage, vascular occlusion, dissection, or significant stenosis. Over the next 48 h, facial weakness progressed to bilateral lower motor neuron facial palsy with mild dysphagia and weak gag reflex, while limb strength remained preserved. Cerebrospinal fluid showed albuminocytologic dissociation. Dedicated contrast-enhanced magnetic resonance imaging of the internal auditory canals showed no facial nerve enhancement; bilateral linear enhancement represented vascular enhancement. Electrodiagnostic testing showed facial motor terminal latency abnormalities, prolonged bilateral blink reflex responses, and facial muscle EMG abnormalities supportive of a facial diplegia GBS variant. Campylobacter testing and anti-ganglioside antibody testing were not performed. He received intravenous immunoglobulin 0.4 g/kg/day for 5 days and gradually improved.

Conclusion: Facial diplegia GBS may initially trigger an acute stroke evaluation when early facial weakness appears unilateral or central. Repeated neurological examination, cerebrospinal fluid analysis, and neurophysiology are essential when persistent symptoms and negative neuroimaging argue against a vascular syndrome.

面部双瘫格林-巴利综合征变体最初表现为卒中模拟:从单侧中央出现的面部无力到双侧面瘫的演变-一个病例报告。
面部双瘫是格林-巴利综合征(GBS)的一种罕见的区域性变异。当面部虚弱表现为单侧或中央型时,最初可能类似于急性脑血管病。病例介绍:一名48岁的斯里兰卡男性,患有未经治疗的高血压、肥胖和新发现的糖尿病,在发病约18小时后出现言语不清和持续的左侧面部无力。初步检查显示左中枢性面瘫,虽然也有不完全的左眼闭眼。在症状出现约25小时后进行非对比计算机断层扫描和当日脑磁共振血管造影,未发现急性梗死、出血、血管闭塞、夹层或明显狭窄。在接下来的48小时内,面部无力进展为双侧下运动神经元面瘫,伴有轻度吞咽困难和微弱的呕吐反射,但肢体力量保持不变。脑脊液显示白蛋白细胞分离。内耳道专用磁共振造影未见面神经增强;双侧线性增强为血管增强。电诊断测试显示,面部运动终末潜伏期异常,双侧眨眼反射反应延长,面部肌肉肌电图异常支持面部双瘫GBS变体。未进行弯曲杆菌检测和抗神经节苷脂抗体检测。静脉注射免疫球蛋白0.4 g/kg/d,持续5天,病情逐渐好转。结论:面部双瘫GBS可在早期出现单侧或中枢性面部无力时触发急性卒中评估。反复的神经学检查、脑脊液分析和神经生理学是必要的,当持续的症状和阴性的神经影像学证明不是血管综合征。
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来源期刊
Case Reports in Neurology
Case Reports in Neurology Medicine-Neurology (clinical)
CiteScore
1.50
自引率
0.00%
发文量
67
审稿时长
14 weeks
期刊介绍: This new peer-reviewed online-only journal publishes original case reports covering the entire spectrum of neurology. Clinicians and researchers are given a tool to disseminate their personal experience to a wider public as well as to review interesting cases encountered by colleagues all over the world. To complement the contributions supplementary material is welcomed. The reports are searchable according to the key words supplied by the authors; it will thus be possible to search across the entire growing collection of case reports with universally used terms, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.
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