The American Psychiatric Association (APA) has updated its Privacy Policy and Terms of Use, including with new information specifically addressed to individuals in the European Economic Area. As described in the Privacy Policy and Terms of Use, this website utilizes cookies, including for the purpose of offering an optimal online experience and services tailored to your preferences.

Please read the entire Privacy Policy and Terms of Use. By closing this message, browsing this website, continuing the navigation, or otherwise continuing to use the APA's websites, you confirm that you understand and accept the terms of the Privacy Policy and Terms of Use, including the utilization of cookies.

×
Site maintenance Monday, July 8th, 2024. Please note that access to some content and account information will be unavailable on this date.
ArticleNo Access

PRESENILE DEMENTIA (ALZHEIMER'S DISEASE)

Its Pathogenesis and Classification With Two Case Reports
Published Online:https://doi.org/10.1176/ajp.102.2.191

Presenile dementia does not appear to be a well-defined clinico-anatomical entity, and single case studies are helpful in elucidating the problem of pathogenesis and classification.

Two cases of presenile dementia are described. One is that of a man who, at the age of 52, developed the typical organic syndrome, with certain signs of focal cortical impairment such as aphasia, paraphasia and disturbances of reading, writing and picture recognition. After severe general deterioration he died at the age of 60, and post-mortem examination revealed the typical histological features of Alzheimer's disease.

The second case is that of a woman who at about the age of 42 began to show unspecific symptoms such as diffuse anxiety, definite phobias and general restlessness, suggestive of a psychoneurosis or the beginning of a functional psychosis. After several years she gradually developed severe disorders of conduct, intellectual and speech impairment. She died in a state of extreme organic dementia and physical deterioration at the age of 48. Post-mortem examination showed severe generalized cortical atrophy (brain weight 864 gms.) with the signs of senility except that the characteristic histological features of Alzheimer's disease were entirely absent.

It has been suggested (Lewy 1925, Spatz 1925) that the process of ageing manifests itself in the central nervous system along two different lines. Atrophy, brown pigment, proliferation of interstitial tissue represent the "primary" phenomena of ageing, and are not confined to the central nervous system or to man. However, the combination of neurofibrillary changes and argentophile plaques is a "secondary" phenomenon of ageing which occurs only in man and in the phylogenetically most recent structures of the nervous system.

The two cases here presented demonstrate that the "primary" and "secondary" phenomena of ageing occur independently. The significance of this fact and its clinical and pathological implications are discussed.

Access content

To read the fulltext, please use one of the options below to sign in or purchase access.