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Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Neuroborreliosis presenting as acute disseminated encephalomyelitis
Ruben Rocha1, Lurdes Lisboa, João Neves
1Pediatric Intensive Care Unit, Centro Hospitalar S João, Porto, Portugal.
Insights
This case study details a 5-year-old boy whose initial symptoms of neuroborreliosis mimicked acute disseminated encephalomyelitis, presenting with neurological deficits. Early diagnosis and treatment are crucial for managing this rare Lyme disease complication.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Neuroimmunology
Background:
- Neuroborreliosis, a Lyme disease manifestation, can present with diverse neurological symptoms.
- Acute disseminated encephalomyelitis (ADEM) is an immune-mediated inflammatory demyelinating disease of the central nervous system.
- Early recognition of neuroborreliosis is critical, as it can mimic other neurological conditions.
Observation:
- A 5-year-old boy presented with acute encephalopathy, facial palsy, and seizures following an upper-airway infection.
- Neurological examination revealed hypotonia, ataxia, dysarthria, and impaired gag/cough reflexes post-mechanical ventilation.
- Brain MRI demonstrated hyperintense lesions in the occipital, parietal, internal capsule, and medulla oblongata.
Findings:
- Polymerase chain reaction (PCR) and Western blotting confirmed Borrelia burgdorferi infection in plasma and cerebrospinal fluid.
- The clinical presentation and MRI findings were consistent with acute disseminated encephalomyelitis as an initial manifestation of neuroborreliosis.
- Diagnosis was supported by laboratory confirmation of Borrelia burgdorferi infection.
Implications:
- This case highlights the importance of considering neuroborreliosis in children presenting with ADEM-like symptoms, especially after potential tick exposure or in endemic areas.
- Prompt antibiotic treatment (ceftriaxone) alongside immunomodulatory therapy (methylprednisolone, immunoglobulin) is essential for managing severe neuroborreliosis.
- Despite treatment, partial neurological recovery underscores the potential for long-term sequelae in pediatric neuroborreliosis, necessitating further research into optimal management strategies.
Abstract:
We report a case of a 5-year-old boy with acute disseminated encephalomyelitis as the initial presentation of neuroborreliosis. Parents report an upper-airway infection a few days before the development of acute encephalopathy, mild facial palsy, and seizures. The patient needed mechanical ventilation for 10 days, and after extubation, he presented hypotonia, ataxia, dysarthria, as well as weak gag and cough reflexes. Brain magnetic resonance imaging showed hyperintense lesions on T2- and fluid-attenuated inversion recovery sequences on the right subcortical occipital and parietal region, left posterior arm of the internal capsule, and in the medulla oblongata. Borrelia burgdorferi was identified in the plasma and cerebrospinal fluid by polymerase chain reaction and in the plasma by Western blotting. He was treated with ceftriaxone, methylprednisolone, and human immunoglobulin. Recovery was partial.
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