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. 2020 Apr 27;140(1):49–62. doi: 10.1007/s00401-020-02160-8

Table 2.

Demographic and neuropathological features of definite cases with LB-Syn+

List of cases Sex Age at LP Age at death Primary NP diagnosis Secondary NP diagnosis McKeith stage Braak stage
Case #1 F 79 79 DLB AD (low) Neocortical 6
Case #2 F 81 81 DLB AD (low) Neocortical 6
Case #3 F 79 81 DLB AD (intermediate) Neocortical 6
Case #4 M 77 77 DLB AD (intermediate) Neocortical 6
Case #5 M 63 65 DLB AD (high) Neocortical 6
Case #6 M 77 77 DLB AD (intermediate) Neocortical 6
Case #7 F 81 81 DLB AD (intermediate) Neocortical 6
Case #8 M 80 80 DLB AD (intermediate) Neocortical 6
Case #9 F 82 83 DLB AD (intermediate) Neocortical 5
Case #10 M 71 72 DLB AD (low) Neocortical 5
Case #11 M 73 73 DLB AD (low) Neocortical 5
Case #12 F 76 77 DLB AD (intermediate), CAA, subcortical arteriosclerotic encephalopathy Limbic 4
Case #13 M 73 73 DLB AD (intermediate), CAA Limbic 4
Case #14 M 83 83 DLB AD (intermediate), CAA Limbic 4
Case #15a M 67 67 sCJD MM1b DLB Neocortical 5
Case #16a F 73 73 sCJD VV2b DLB, AD (intermediate), CAA Neocortical 5
Case #17a F 75 76 Primary CNS lymphoma PARTc Limbic 4
Case #18a M 87 87 Metabolic encephalopathy AD (low), lacunar stroke Brainstem 3
Case #19a M 72 73 sCJD VV2b AD (low) Brainstem 2
Case #20a M 81 81 sCJD MV2K + 2Cb AD (low) Brainstem 1
Case #21a F 65 65 sCJD MM1b None Brainstem 1

LP lumbar puncture, NP neuropathologic, DLB dementia with Lewy bodies, AD Alzheimer’s disease, CAA cerebral amyloid angiopathy, CNS central nervous system, sCJD sporadic Creutzfeldt–Jakob disease, PART primary age-related tauopathy

aDementia with incidental LB co-pathology

bsCJD subtypes were defined in accordance with Parchi et al. [47]

cPART was diagnosed according to Crary et al. [18]