Magnetic Resonance Imaging Follow-up in Creutzfeldt-Jakob Disease
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The history of a 67-year-old woman with histologically proven Creutzfeldt-Jakob disease (CJD) is presented. Before typical clinical and neurophysiological signs of CJD developed, magnetic resonance imaging (MRI) showed slightly enhanced signal intensity of the caudate nuclei and putamina in T2-weighted and proton density images, corresponding to spongiform degeneration in neuropathological examination. Five weeks later characteristical progressive cortical atrophy was demonstrated by follow-up MRI.
Radiological assessment of Creutzfeldt-Jakob disease.
Tschampa H, Zerr I, Urbach H Eur Radiol. 2006; 17(5):1200-11.
PMID: 17093966 DOI: 10.1007/s00330-006-0456-2.
Serial MRI in early Creutzfeldt-Jacob disease with a point mutation of prion protein at codon 180.
Ishida S, Sugino M, Koizumi N, Shinoda K, OHSAWA N, Ohta T Neuroradiology. 1995; 37(7):531-4.
PMID: 8570047 DOI: 10.1007/BF00593711.