[Clinical and morphologic characterization of Pick's dementia: case report and review of the literature].
Valery V LitvinovG G FreindPublished in: Arkhiv patologii (2024)
Diseases morphologically characterized by frontotemporal lobar degeneration have relatively recently been considered as a group of frontotemporal dementias. This group is characterized by a tendency to early clinical onset of dementia, common genetic and morphological features, as well as a possible association with diseases such as amyotrophic lateral sclerosis and atypical parkinsonism syndrome. Historically, Pick's dementia (Pick's disease) was described as the first of the frontotemporal dementias, which is morphologically characterized by the presence of argyrophilic Pick's bodies represented by 3R-tau protein in the neurons of the cerebral cortex. Despite the characteristic clinical and morphological picture due to the relative rarity, the diagnosis of Pick's dementia is infrequently made by both clinicians and pathologists. The article presents current data on frontotemporal dementia. A case of Pick's dementia with characteristic clinical manifestations in the form of early onset of behavioral and personality disorders, as well as specific morphological changes in the brain, is described.
Keyphrases
- amyotrophic lateral sclerosis
- mild cognitive impairment
- early onset
- cognitive impairment
- late onset
- spinal cord
- genome wide
- dna methylation
- multiple sclerosis
- electronic health record
- small molecule
- white matter
- copy number
- brain injury
- cerebral ischemia
- parkinson disease
- blood brain barrier
- deep brain stimulation
- protein protein