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Acute encephalopathy with bilateral thalamotegmental involvement and a benign course: a case report from Brazil
Regina Maria Papais Alvarenga1, Vanderson Carvalho Neri, Tatiane Mendonça
1Department of Neurology, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil. regina_alvarenga@hotmail.com
Insights
This rare acute postinfectious encephalopathy in children, often fatal, can be treated. A Brazilian child recovered fully after methylprednisolone therapy for severe brain lesions.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Acute postinfectious encephalopathy is a rare neurological condition typically affecting children.
- It often follows a respiratory infection and fever, progressing to severe outcomes like coma in most cases.
Observation:
- A case report details a Brazilian child of African descent presenting with fever, headache, and bilateral visual loss.
- The child progressed to coma with pyramidal signs and convulsions, exhibiting diffuse, symmetrical thalamotegmental and brainstem lesions on MRI.
Findings:
- The patient received methylprednisolone, leading to clinical improvement and regression of brain lesions.
- This resulted in a favorable outcome with no neurological sequelae, which is atypical for this condition.
Implications:
- This case highlights the potential efficacy of methylprednisolone in treating severe acute postinfectious encephalopathy.
- The favorable outcome in this atypical presentation suggests that prompt treatment can prevent long-term neurological deficits.
Abstract:
This rare encephalopathy that generally affects children is preceded by a respiratory infection and fever associated with convulsions and may progress to coma. Outcome is catastrophic in most cases. This case report describes a Brazilian child of African descent with fever, cephalea and bilateral amaurosis, who evolved to coma with pyramidal signs and associated convulsions. MRI showed diffuse, symmetrical lesions in the thalamotegmental region and brainstem. Following administration of methylprednisolone, the clinical condition of the patient improved and the brain lesions regressed, leaving the child with no current neurological deficits. This was a case of acute postinfectious encephalopathy, involving various brain structures. Outcome was favourable with no sequelae following therapy. This case was atypical due to the bilateral visual involvement and extensive encephalic lesions in a child of African descent with no neurological sequelae following therapy. No other similar cases have been reported in the literature.
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