| Literature DB >> 26401927 |
Jia Liu1, Ming-wei Zhu2, Thomas Arzberger3,4,5, Lu-ning Wang2.
Abstract
A clinicopathological investigation was conducted on a case of an 89-year-old man with a 10-year history of progressive dementia who also suffered strokes, apathy, aphasia, dysarthria, weakness of both legs, and walking difficulties. At autopsy, we found an obvious atrophy of the frontal and temporal cortex. Lewy bodies (LBs) could be seen in brain stem, amygdala, and neocortex. Argyrophilic grains were observed in hippocampus, entorhinal cortex, neocortex, amygdala, and pons, as well as neurofibrillary tangles in the entorhinal cortex and hippocampus. The case presented here is a rare case of frontotemporal lobar degeneration with accumulation of argyrophilic grains and Lewy bodies.Entities:
Keywords: Argyrophilic grains; FTLD-tau; Lewy bodies; frontotemporal lobar degeneration
Mesh:
Year: 2015 PMID: 26401927 DOI: 10.3233/JAD-150225
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472