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A Rare Case Report of Benign Intracranial Hypertension Caused by Hypervitaminosis A
Hanane Hajaj1,2, Ayad Ghanam1,2, Hind Zahiri1,2
1Pediatrics, Faculty of Medicine and Pharmacy, Mohammed I University of Oujda, Oujda, MAR.
Insights
Benign intracranial hypertension (BIH) in children can be caused by vitamin A toxicity. Early diagnosis and treatment are crucial for recovery, as demonstrated in a case study of a 13-year-old girl.
Area of Science:
- Pediatrics
- Neurology
- Toxicology
Background:
- Benign intracranial hypertension (BIH) is characterized by elevated intracranial pressure without identifiable mass lesions or hydrocephalus.
- Typical symptoms include headache, papilledema, and potential sixth nerve palsy, though presentation can vary.
- While often idiopathic, rare causes like vitamin A toxicity warrant consideration.
Observation:
- A previously healthy 13-year-old girl presented with photophobia, headache, vomiting, and bilateral papilledema.
- Neurological imaging (MRI, CT) and cerebrospinal fluid analysis were normal.
- Elevated serum vitamin A levels were identified as the sole positive laboratory finding.
Findings:
- The patient was diagnosed with BIH and successfully treated with acetazolamide.
- Papilledema regressed, and symptoms resolved within two weeks.
- This case highlights vitamin A toxicity as a treatable cause of BIH in children.
Implications:
- Clinicians should consider vitamin A toxicity in pediatric cases of BIH with papilledema and normal neuroimaging.
- Prompt evaluation of vitamin A levels can lead to effective treatment and prevent long-term complications.
- This underscores the importance of a comprehensive differential diagnosis in pediatric neurology.
Abstract:
Benign intracranial hypertension (BIH) in children is recognized as elevated intracranial pressure without hydrocephalus or intracranial mass. It manifests differently in adults, with no apparent predilection for sex or weight. Headache, papilledema, and possibly sixth nerve palsy with visual field defects are the typical symptoms of this syndrome. Vitamin A toxicity is a rare cause of BIH. We report the case of a previously healthy 13-year-old girl presenting with photophobia, a frontal headache, and vomiting. She had bilateral papilledema discovered by fundoscopy. Both magnetic resonance imaging and brain CT were normal. At admission, a lumbar puncture (LP) revealed an opening pressure of 26 cm H2O with normal cerebrospinal fluid (CSF) analysis. The diagnosis of BIH was established, and treatment with acetazolamide was started, with good clinical results. Regular eye evaluations showed a regression of papilledema. Elevated serum vitamin A levels were the only positive findings. Within two weeks, the patient was discharged without any symptoms. This study aims to attract the attention of clinicians to the importance of evaluating vitamin A toxicity in the context of papilledema and oculomotor problems in a child who has undergone normal neuroradiological investigations.
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