The provisional criteria proposed in 1985 by Khachaturian et al. empha
sized numbers of plaques and neglected tangles, as did CERAD (Consorti
um to Establish a Registry for Alzheimer's Disease). The decision to s
et an arbitrary number of plaques as ''pathologic'' assumed that some
neuritic plaques are a normal phenomenon in the aging brain. Neuritic
plaques and neurofibrillary tangles are age-related lesions, but they
are pathologic (i.e., lesions) no matter how many there are. In a clin
ically demented patient without vascular or other neurodegenerative le
sions, a clinico-pathologic diagnosis of AD (a clinico-pathologic enti
ty) can be made with a high level of confidence by demonstrating, and
without counting, plaques and tangles. The vast majority of AD cases a
re straightforward, and diagnostic lesions can be appreciated with a s
imple silver stain. If patients' histories are unknown or uncertain, t
he clinical significance of the observed plaques and tangles must rema
in debatable. This is the essence of the consensus statement with whic
h I wholeheartedly agree. In such cases without a dementia history, on
e can offer a neuropathologic diagnosis of Senile or Pre-senile Cerebr
al Disease (not ''dementia'') of the Alzheimer type. Precise clinico-p
athologic correlations and some quantitative measures are needed for e
lucidating the pathogenesis of AD and for establishing a primary demen
ting diagnosis when AD is mixed with other dementing diseases. These c
orrelations must be based on periodic and fairly extensive neuropsycho
logical testing followed shortly thereafter by a detailed postmortem n
europathologic evaluation. (C) 1997 Elsevier Science Inc.