[Brain stem encephalitis in childhood]
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Updated: Oct 29, 2026

Intracerebroventricular and Intravascular Injection of Viral Particles and Fluorescent Microbeads into the Neonatal Brain
Published on: July 24, 2016
I Bodegas1, A Martínez-Bermejo, M J García de Miguel
1Servicio de Neurología, Hospital Infantil La Paz, Madrid, España.
Insights
Post-infectious encephalitis of the brain stem (ETC) is rare in infants. Early diagnosis and treatment are crucial due to high mortality and potential for severe neurological deficits.
Area of Science:
- Pediatric Neurology
- Infectious Diseases
- Neuroimaging
Background:
- Post-infectious encephalitis of the brain stem (ETC) is an uncommon condition, particularly in infants.
- Prompt recognition and management are vital due to the potential for severe outcomes.
Observation:
- Two infant cases (4 and 9 months) presented with subacute onset after a catarrhal illness.
- Clinical features included ataxia, altered consciousness, pyramidal tract signs, and cranial nerve palsies.
- MRI revealed pontine lesions, though not always correlating with clinical severity.
Findings:
- One infant recovered without sequelae.
- The second infant experienced persistent cranial nerve deficits and gait abnormalities.
- Clinical courses varied significantly between the two patients.
Implications:
- Highlights the rarity of ETC in infancy, necessitating a high index of suspicion.
- Emphasizes the importance of early empirical treatment, especially if herpes simplex virus is suspected, due to high mortality and sequelae risks.
Objective:
To present two cases of post-infectious encephalitis of the brain stem (ETC) in infancy, which is very infrequent at this age.
Clinical Cases:
Two patients aged 4 months and 9 months respectively had a previous history of a catarrhal illness a few days before the onset of encephalitis. The clinical condition was of subacute onset and torpid course, characterized by ataxia, reduced level of consciousness, involvement of the pyramidal tracts and paralysis of the cranial nerves. No significant information for the diagnosis of either case was obtained from CT. MR showed lesions at the level of the pons. However, the MR image did not correspond in seventy to the clinical condition. The clinical courses of the two patients were different. One case recovered with no sequelae. In the other case the cranial nerves and gait did not return to normal.
Conclusions:
In our experience, ETC is rarely seen in infancy. A high degree of suspicion and early treatment of ETC caused by the herpes simplex virus is necessary, since there is usually a high mortality or serious neurological sequelae.
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