Literature DB >> 26401927

Frontotemporal Lobar Degeneration with Accumulation of Argyrophilic Grains and Lewy Bodies: A Clinicopathological Report.

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


  1 in total

1.  A novel SNCA E83Q mutation in a case of dementia with Lewy bodies and atypical frontotemporal lobar degeneration.

Authors:  Alifiya Kapasi; Jared R Brosch; Kelly N Nudelman; Sonal Agrawal; Tatiana M Foroud; Julie A Schneider
Journal:  Neuropathology       Date:  2020-08-12       Impact factor: 1.906

  1 in total

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