

Creutzfeldt-Jakob Disease (CJD)
- Progressive, fatal spongioform encephalopathy
- Transmissable disease
- Clinical: rapidly progressive dementia (<2>
- Distribution of abnormality: usually symmetric, deep gray nuclei (caudate head, putamen, thalamus), cerebral cortex
- Characters: high signal on T2 and FLAIR, restricted diffusion on DWI
- DWI may be the most sensitive imaging method for the early clinical diagnosis of CJD
Shiga Y, et al. Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease. Neurology 2004;63:443-449.