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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: Ann Neurol. 2017 Jan;81(1):79–92. doi: 10.1002/ana.24833

Table 4.

Final neuropathological diagnosis of cases with rapidly progressive other neurological disorders (OND) clinically suspected from prion disorder.

Neuropathological diagnosis N %
Alzheimer disease (AD) 34 41.5
Multi-infarct dementia 7 8.5
AD with multi-infarcts 6 7.3
AD with Lewy bodies 5 6.1
CNS Lymphoma 4 4.9
Frontotemporal lobar degeneration 4 4.9
Lewy body dementia 4 4.9
Leucodystrophy 4 4.9
Primary angiitis 2 2.4
Progressive multifocal leucoencephalopathy 2 2.4
Coccidiomycosis 1 1.2
Diffuse leucoencephalopathy with axonal spheroids 1 1.2
Encephalitis 1 1.2
Focal necrotizing encephalopathy 1 1.2
Global ischemic encephalopathy 1 1.2
Granulomatous amoebic encephalitis 1 1.2
Hemorrhagic stroke 1 1.2
Leptomeningeal carcinomatosis 1 1.2
Malignant glioma 1 1.2
Wernicke-Korsakoff syndrome with olivary gliosis 1 1.2
Undetermined 1 1.2
Total 82 100
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