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Pseudotumoral acute hemicerebellitis in a child
Rita B Morais1, Inês Sousa, Maria J Leiria
1Department of Pediatrics, S. Francisco Xavier Hospital, Estrada do Forte do Alto do Duque, 1495-005 Lisbon, Portugal. ritabmorais@gmail.com
Insights
Acute cerebellitis, an inflammation of the cerebellum, is rare in children. This case highlights that hemicerebellitis, even without typical symptoms, may require surgery.
Area of Science:
- Pediatric Neurology
- Neuroinflammation
- Neuroradiology
Background:
- Acute cerebellitis is a cerebellar inflammatory disorder.
- Hemicerebellitis, a rare form, can mimic brain tumors in children.
- Surgical intervention for hemicerebellitis is seldom reported.
Observation:
- A 15-year-old presented with headache, not cerebellar signs.
- CT showed a mass compressing the fourth ventricle.
- MRI revealed left cerebellar swelling, hydrocephalus, and tonsillar herniation.
Findings:
- The patient underwent decompressive craniectomy due to symptom progression.
- Biopsy confirmed an inflammatory process, likely viral.
- Post-surgery, the patient recovered with only mild cerebellar atrophy.
Implications:
- This case underscores the atypical presentations of acute cerebellitis.
- It demonstrates the potential need for surgical intervention in severe cases.
- Early diagnosis and management are crucial for favorable outcomes.
Abstract:
Acute cerebellitis is an inflammatory disorder usually involving both sides of the cerebellum and presenting with localized signs such as ataxia. Hemicerebellitis is extremely rare in children and may clinically and radiologically resemble a tumor. There are very few reports of hemicerebellitis needing decompressive surgery. We report a case of hemicerebellitis in a 15 year old child presenting with severe headache but no cerebellar symptoms whose brain CT revealed an ill-defined mass compressing the fourth ventricle (pseudotumoral). MRI of the posterior fossa revealed a swollen left cerebellar hemisphere, supra-tentorial hydrocephalus and tonsil herniation, without any cerebral or brain stem lesions. Due to worsening symptoms she required a decompressive craniectomy, and the biopsy revealed an inflammatory process, possibly viral. At follow-up she was asymptomatic and the MRI revealed only slight cerebellar atrophy. This case had an atypical clinical presentation and illustrates that though a self-limited evolution is expected, surgical intervention may be needed in acute cerebellitis.
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