123I-ioflupane SPECT scan in a patient with Creutzfeldt-Jakob disease.
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A 62-year-old woman presented with gait ataxia, bradykinesia, bilateral rigidity, choreic and dystonic movements, and psychomotor slowing. Magnetic resonance imaging (MRI) (Fig. 1), EEG and CSF analysis were compatible with a diagnosis of Creutzfeldt-Jakob disease (CJD). The 123I-ioflupane SPECT (Fig. 2) was normal, indicating the relative sparing of nigro-striatal fibers and suggesting that her movement disorder was due to postsynaptic
[1] L. Trojano,et al. Striatal [123I] FP‐CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt–Jakob disease , 2009, Acta neurologica Scandinavica.
[2] R. Sciot,et al. Sparing of the substantia nigra in sporadic Creutzfeldt‐Jakob disease presenting as an acute corticobasal syndrome , 2007, Movement disorders : official journal of the Movement Disorder Society.
[3] K. Ikeda,et al. Sporadic Creutzfeldt-Jakob disease: Magnetic resonance imaging and clinical findings , 2005, Neurology.