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Published on: October 12, 2012
Agranulocytosis following phenytoin-induced hypersensitivity syndrome
Susumu Ito1, Mutsuki Shioda, Kaori Sasaki
1Department of Pediatrics, School of Medicine, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, Japan. susumu.ito@nifty.com
Insights
Phenytoin can cause antiepileptic drug hypersensitivity syndrome (AHS). A rare case showed AHS progressing to agranulocytosis, a serious condition requiring prompt medical intervention.
Area of Science:
- Pharmacology
- Immunology
- Hematology
Background:
- Phenytoin is a widely used antiepileptic medication.
- Antiepileptic drug hypersensitivity syndrome (AHS) is a rare but severe complication associated with phenytoin use.
Observation:
- A 5-year-old boy experienced typical AHS symptoms including fever, rash, lymphadenopathy, and hepatitis after phenytoin treatment.
- Following recovery from initial AHS symptoms, the patient unexpectedly developed agranulocytosis with fever.
Findings:
- The patient's AHS presentation lacked eosinophilia and lymphocytosis.
- Successful treatment involved high-dose steroids for AHS and a combination of immunoglobulin, granulocyte colony-stimulating factor, and cefepime for agranulocytosis.
Implications:
- This case highlights a potential, severe progression from AHS to agranulocytosis.
- Recognizing this unexpected complication is crucial for managing phenytoin-induced adverse reactions and preventing life-threatening outcomes.
Abstract:
Phenytoin, one of the most common antiepileptic drugs, is a major cause of antiepileptic drug hypersensitivity syndrome (AHS), which is a rare but potentially fatal complication. We herein report a 5-year-old boy who developed unexpected agranulocytosis with fever approximately one week after recovering from the typical symptoms of AHS, characterized by fever, rash, lymphadenopathy, and hepatitis, but lacking eosinophilia or lymphocytosis. High-dose steroid therapy for the former symptoms of AHS, and immunoglobulin, granulocyte colony-stimulating factor, and cefepime for the latter agranulocytosis were successfully performed. This unexpected progression from AHS to agranulocytosis shortly after recovering from the former should be recognized as another risk of AHS, possibly leading to a life-threatening condition.
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