Neuroborreliosis Presenting as Guillain-Barré Syndrome
- PMID: 37614265
- PMCID: PMC10443435
- DOI: 10.7759/cureus.42322
Neuroborreliosis Presenting as Guillain-Barré Syndrome
Abstract
Lyme disease (LD) is the most common vector-borne disease in the United States. The early localized disease presents with erythema migrans and nonspecific constitutional symptoms. A neurological manifestation of LD (neuroborreliosis) is only seen in 10-15% of LD cases, and it typically presents as cranial neuritis or painful radiculitis. We report a case of a 33-year-old male who presented with progressive ascending bilateral lower extremities weakness with paresthesia in hands and feet following an upper respiratory tract infection and an abdominal rash. Cerebrospinal fluid (CSF) analysis revealed albuminocytologic dissociation. An electrodiagnostic study showed prolonged distal motor latency, conduction block, and absent F-wave response. Magnetic resonance imaging of the lumbar spine revealed enhancement of the cauda equina nerve roots. After a lack of improvement with intravenous immunoglobulin for presumed Guillain-Barré syndrome (GBS), Lyme serologies were sent and showed positive Lyme antibodies in serum and CSF as well as positive western blot IgM followed by IgG seroconversion a week later. The patient was started on IV ceftriaxone and doxycycline for four weeks with significant improvement in his symptoms. This is a rare case of LD presenting as GBS. Lyme can have diverse neurologic manifestations and should be considered in the differential diagnosis of GBS in the appropriate settings.
Keywords: albuminocytologic dissociation; ascending paralysis; borrelia burgdorferi; demyelination; guillain-barré syndrome; guillain-barré syndrome (gbs); lyme disease; neuroborreliosis; tick; western blot.
Copyright © 2023, Farr et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
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