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Abstract We report the first autopsy case of MM1‐type sporadic Creutzfeldt–Jakob disease (sCJD) who survived 80 months after long‐term artificial ventilatory support. The cerebral cortex and white matter exhibited severe atrophy, sparing the hippocampus. The prion protein aggregates of 10–20 μm in diameter were prominent. The structure consisted of granulofilamentous profiles. This case provides clues on how MM1‐type sCJD extends pathologically after a long clinical course.
Kawanami et al. (Wed,) studied this question.
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