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Listeria monocytogenes Infection of the Brain
Published on: October 2, 2018
Delayed Hydrocephalus Following Listeria monocytogenes Meningitis in an Immunocompetent Child
Diana Guzmán García1, Andrea A Sánchez Salgado1, Jorge A Sánchez López1
1Pediatrics, Hospital Regional, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE), Monterrey, MEX.
Insights
Listeria meningitis in children can lead to delayed hydrocephalus even after initial recovery. Prompt diagnosis, targeted antibiotics, and close neurological monitoring are crucial for managing this severe central nervous system infection.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Neuroimaging
Background:
- Listeria monocytogenes meningitis is a severe CNS infection in immunocompetent children.
- Early recognition and treatment are vital.
Abstract:
Listeria monocytogenes meningitis in immunocompetent pediatric patients may present as a severe central nervous system infection and requires prompt recognition and appropriate antimicrobial therapy. We report the case of a previously healthy twelve-year-old boy who presented with acute-onset fever, severe holocranial headache, nausea, and recurrent vomiting consistent with bacterial meningitis. Given his stable neurological examination without focal deficits or signs of increased intracranial pressure, brain magnetic resonance imaging was performed as the initial neuroimaging study and demonstrated diffuse leptomeningeal enhancement without ventricular dilation, with radiologic findings compatible with ependymitis. Empiric intravenous ceftriaxone and vancomycin were initiated. Cerebrospinal fluid culture subsequently confirmed Listeria monocytogenes, and antimicrobial therapy was adjusted to targeted intravenous ampicillin, resulting in defervescence within 48 hours, complete resolution of headache and vomiting, and a progressive decrease in inflammatory markers. One week after hospital discharge, the patient returned with worsening headache, persistent vomiting, and anisocoria, consistent with acute increased intracranial pressure. A non-contrast head computed tomography scan performed at a secondary-level medical unit revealed obstructive hydrocephalus. Given the presence of neurological deterioration and radiological findings, repeat imaging was not performed, and the patient was transferred directly to the operating room for urgent ventriculoperitoneal shunt placement. The postoperative course was favorable, with resolution of anisocoria and progressive improvement in headache and vomiting. Neurological stability was maintained during follow-up. This case highlights the potential for delayed hydrocephalus following apparent clinical recovery from Listeria meningitis and underscores the importance of microbiological confirmation, timely antimicrobial adjustment, and structured neurological follow-up.

