Abstract
The principles for classification of organic dementia are based on our present knowledge of its etiology, clinical picture, and pathological characteristics such as the type and predominant location of the brain damage. This paper concerns the clinical and pathological findings in dementia cases with primary degenerative changes within the frontal and temporal lobes and the possibility to differentiate this frontotemporal dementia (FTD) from Alzheimer’s disease (AD) and other dementias. The importance of localized cortical atrophy within the frontal and temporal lobes in dementia was pointed out by Arnold Pick more than 100 years ago [1]. The neuropathological characteristics of this condition were given by Alzheimer [2], who described the ballooned cells and argentophilic inclusion bodies. The clinicopathological entity of this “Pick’s disease” or “lobar atrophy” was delineated by Onari and Spatz [3] and Schneider [4], and further elaborated in a series of important contributions [5–9].
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Gustafson, L., Brun, A. (1999). Frontotemporal Dementia. In: Govoni, S., Bolis, C.L., Trabucchi, M. (eds) Dementias. Springer, Milano. https://doi.org/10.1007/978-88-470-2149-5_7
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