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Published on: September 20, 2024
Hepatic failure in a child with anti-epileptic hypersensitivity syndrome
Albert M Li1, Edmund As Nelson, Ellis K L Hon
1Department of Paediatrics, Prince of Wales Hospital, Chinese University of Hong Kong, Shatin, Hong Kong. albertmli@cuhk.edu.hk
Insights
A child experienced a severe hypersensitivity reaction to phenobarbitone, leading to liver failure and respiratory symptoms. Treatment with immune globulin and corticosteroids helped manage the reaction and aided recovery.
Area of Science:
- Pediatric Medicine
- Pharmacology
- Hepatology
Background:
- Phenobarbitone is an anticonvulsant medication with known risks of hypersensitivity reactions.
- Severe hypersensitivity reactions can manifest with multi-organ involvement.
- Fulminant hepatic failure is a rare but life-threatening complication of drug reactions.
Observation:
- An 11-year-old boy presented with severe hypersensitivity to phenobarbitone, progressing to fulminant hepatic failure.
- The patient subsequently developed symptoms consistent with severe acute respiratory syndrome (SARS).
- The SARS-like illness potentially complicated the management and recovery from the initial hypersensitivity reaction.
Findings:
- The hypersensitivity reaction to phenobarbitone was the primary cause of the severe illness.
- The co-occurrence of SARS-like symptoms presented a diagnostic and therapeutic challenge.
- Intravenous immune globulin and corticosteroids were effective in controlling the hypersensitivity reaction.
Implications:
- This case highlights the potential for severe, multi-systemic reactions to phenobarbitone in children.
- The interplay between drug hypersensitivity and infectious/syndromic illnesses requires careful consideration in clinical practice.
- Prompt and aggressive immunosuppressive therapy can be crucial for managing severe hypersensitivity reactions.
Abstract:
An 11-year-old boy developed severe hypersensitivity reaction to phenobarbitone resulted in fulminant hepatic failure. During the course of illness, he developed clinical features compatible with severe acute respiratory syndrome (SARS) that may have complicated the recovery of his underlying hypersensitivity reaction, which was subsequently controlled with intravenous immune globulin and corticosteroids.
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