One-year-old boy with refractory Listeria monocytogenes meningitis due to persistent hypercytokinemia

Shuya Kaneko1, Kiyoshi Hatasaki1, Kazuyuki Ueno1

  • 1Department of Pediatrics, Toyama Prefectural Central Hospital, Toyama, Japan.

Insights

Listeria monocytogenes meningitis can cause severe hypercytokinemia and hemophagocytic lymphohistiocytosis in children. Corticosteroid therapy, alongside antibiotics, may be crucial for resolving neurological symptoms and persistent fever.

Area of Science:

  • Pediatric Neurology
  • Infectious Diseases
  • Immunology

Background:

  • Listeria monocytogenes (LM) meningitis is a serious infection, particularly in infants.
  • Hypercytokinemia and hemophagocytic lymphohistiocytosis (HLH) are potential complications.
  • Neurological sequelae can arise from severe LM meningitis.

Observation:

  • A healthy 22-month-old boy developed LM meningitis with fever, vomiting, altered consciousness, and extraocular muscle paralysis.
  • Brain MRI showed bilateral deep white matter lesions.
  • Despite initial antibiotic treatment, persistent fever and elevated inflammatory cytokines (neopterin) were observed for 40 days.

Findings:

  • Antibiotic therapy alone was insufficient to resolve persistent hypercytokinemia and neurological symptoms.
  • Long-term corticosteroid administration, specifically dexamethasone, was required.
  • Dexamethasone effectively treated neurological deficits including consciousness disturbance and extraocular muscle paralysis.

Implications:

  • Listeria monocytogenes meningitis can manifest with encephalopathy and prolonged fever due to hypercytokinemia.
  • Corticosteroid therapy should be strongly considered in managing complex LM meningitis cases with hypercytokinemia and neurological involvement.
  • This case highlights the importance of a multimodal treatment approach for severe LM meningitis.

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