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.
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.
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.