We report on a 3-year-old girl with respiratory syncytial virus (RSV) encep
halitis manifested by disturbance of consciousness, conjugate eye deviation
, anuria, truncal ataxia and intention tremor. T2-weighted magnetic resonan
ce imaging (MRI) showed hyperintense areas in the cerebellar cortex. No les
ion was detected in the cerebral cortex, pens or spinal cord. The hyperinte
nse areas in the cerebellar cortex diminished with recovery from the clinic
al manifestations and had resolved 2 months after onset. The MRI lesions in
the cerebellum were considered to be due to oedema. SPECT and positron emi
ssion tomography (PET), performed 3 months after onset, disclosed areas of
hypoperfusion and hypometabolism at the same sites. One year after onset, M
RI showed mild atrophy of the cerebellum. Hypoperfusion on SPECT and hypome
tabolism on PET remained. Neuroimaging showed that ataxia and tremor in thi
s case were the result of cerebellitis, The patient has no neurological def
icit except for mild truncal ataxia. This patient is a rare example of RSV
encephalitis.