Case report details progressive dysphagia and paresthesias in a male patient, suggesting an unusual Guillain-Barré subtype.
Objective: To report a case of a patient with Pharyngo-Cervico-Brachial syndrome, as an unsual variant of GuillainBarre Syndrome. Methods: Patient data were obtained from medical records from “Clí nica Universidad de Navarra”, Pamplona, Spain. Results: We report the case of a 41-year-old male with no relevant medical history or recent vaccinations, who presented to the emergency department with a 24-hour history of progressive dysphagia, dysarthria, choking episodes, and ascending paresthesias involving the limbs and tongue. Neurological examination revealed moderate dysarthria, nasal voice, weakness of soft palate elevation, and generalized areflexia, without motor or sensory deficits in the limbs or ocular motility impairment. Persistent tachycardia was observed during hospitalization. Brain MRI was unremarkable. Cerebrospinal fluid analysis revealed albumin-cytological dissociation. Anti-ganglioside antibodies (anti-GT1a, anti-GT1b, and anti-GQ1b) were detected. Electrophysiological studies showed a mild reduction in motor and sensory nerve conduction amplitudes in the upper limbs, with normal findings in the lower limbs. The patient received intravenous immunoglobulin (2 g/kg over 5 days) with good tolerance and progressive clinical improvement.
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Javier Urmeneta Ulloa (2025) studied this question.
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