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Updated: Aug 17, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
[Acute leukoencephalitis in infant treated by high-dose corticosteroid. A case report]
Sonia Halioui-Louhaichi1, Wissal Ben Jmaa, Sarra Briki
1Service de Pédiatrie, CHU Mongi Slim, la Marsa, Tunisie.
Insights
Acute post-infectious leukoencephalitis is a rare condition. This case study highlights a pediatric patient who recovered after high-dose corticosteroid therapy for this neurological disorder.
Area of Science:
- Pediatric Neurology
- Neuroimmunology
- Infectious Diseases
Background:
- Acute post-infectious leukoencephalitis (APLE) is a rare, immune-mediated demyelinating disease affecting the central nervous system.
- It typically occurs after a viral infection and presents with neurological deficits.
Observation:
- A 2.5-year-old child presented with fever, rapid deterioration, obtundation, coma, and cranial nerve palsies (6th and 7th).
- Cerebrospinal fluid analysis revealed lymphocytosis with negative cultures.
- Head MRI showed diffuse T2-weighted white matter hyperintensities, confirming the diagnosis.
Findings:
- The patient was diagnosed with acute post-infectious leukoencephalitis based on clinical presentation, CSF findings, and MRI.
- Treatment with high-dose corticosteroids led to a positive clinical response.
Implications:
- This case underscores the importance of considering APLE in children with acute neurological deterioration post-infection.
- Prompt diagnosis and aggressive immunomodulatory treatment, such as corticosteroids, can be effective in managing APLE.
- Further research into the specific triggers and long-term outcomes of APLE is warranted.
Abstract:
The authors report a case of acute post infectious leukoencephalitis observed in a tow-years and a half children admitted to our hospital for fiver with suddent condition deterioration, obnibulation, coma and paralysis of the 6th and 7th cranial nerve. Cerebrospinal fluid study showed lymphocytosis with negative culture. Head magnetic resonance imaging demonstrated diffuse high signals over the white matter on T2 weighted images so the diagnosis was confirmed. High dose corticosteroid therapy was effective.
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