A 25-year-old woman was admitted to our hospital with encephalopathy and cl
inical signs of cerebellar dysfunction. She had recently received an overdo
se of phenytoin. On admission, plasma phenytoin level was high (50 mu g/ml,
therapeutic range 10-20 mg/ml). Magnetic resonance imaging showed no signs
of cerebellar atrophy. The patient's neurological condition improved rapid
ly after withdrawal of phenytoin. Eight months later, the neurological exam
ination disclosed minimal cerebellar disorders and magnetic resonance imagi
ng showed cerebellar atrophy. Cerebellar atrophy due to acute phenytoin int
oxication is very unusual but few cases have been reported. The present cli
nical and radiological findings suggest that short-term phenytoin overdose
alone may cause cerebellar atrophy.