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Pseudotumour cerebri due to phenytoin in a child
Sabitha Sasidharan Pillai1, Arakkal Riyaz1,2, Chakkiyar Krishnan1
1Department of Pediatrics, Government Medical College, Calicut, Kerala, India.
Insights
This case report highlights phenytoin-induced pseudotumour cerebri in a child. Prompt withdrawal of phenytoin resolved symptoms, emphasizing its importance in diagnosing drug-induced intracranial hypertension.
Area of Science:
- Neurology
- Pediatrics
- Ophthalmology
Background:
- Pseudotumour cerebri, or idiopathic intracranial hypertension, is characterized by elevated intracranial pressure without a clear cause.
- Phenytoin is an anticonvulsant medication commonly used for seizure prophylaxis.
Observation:
- A 9-year-old boy developed headache and diplopia after receiving phenytoin for seizure prophylaxis post-surgery for Langerhans cell histiocytosis.
- Clinical examination revealed bilateral sixth nerve palsy, and cerebrospinal fluid pressure was elevated.
Findings:
- Phenytoin administration was causally linked to the development of pseudotumour cerebri in this pediatric patient.
- Discontinuation of phenytoin led to complete resolution of the patient's symptoms and neurological deficits.
Implications:
- This case underscores the importance of considering drug-induced aetiologies, specifically phenytoin, in pediatric patients presenting with signs of intracranial hypertension.
- Early recognition and withdrawal of the offending agent are crucial to prevent potential vision loss and other complications associated with prolonged elevated intracranial pressure.
Abstract:
Pseudotumour cerebri is a manifestation of intracranial hypertension in an otherwise normal individual. We hereby report phenytoin-induced pseudotumour cerebri in a 9-year-old boy who received phenytoin as a prophylactic anticonvulsant following surgical removal of unifocal Langerhans cell histiocytosis involving the right frontal bone. The child was evaluated for headache and diplopia after starting phenytoin and on evaluation was found to have bilateral sixth nerve palsy. The only abnormality detected was an elevated cerebrospinal fluid pressure. Withdrawal of phenytoin resulted in complete resolution of symptoms. Despite meticulous literature search, we found only 1 other report of phenytoin induced pseudotumour cerebri. We report this case to highlight the need to consider this entity whenever a patient presents with new onset or persistent headache and visual symptoms soon after starting a medication since a high degree of suspicion is needed to arrive at the diagnosis and to take appropriate steps before it progresses to harmful complications such as vision loss.
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