Progressive supranuclear palsy presenting with primary progressive aphasia—Clinicopathological report of an autopsy case

2003 ◽  
Vol 105 (6) ◽  
pp. 610-614 ◽  
Author(s):  
A. Mochizuki ◽  
Y. Ueda ◽  
Y. Komatsuzaki ◽  
K. Tsuchiya ◽  
T. Arai ◽  
...  
2020 ◽  
Vol 15 (5) ◽  
pp. 511-522 ◽  
Author(s):  
Casey L Brown ◽  
Alice Y Hua ◽  
Lize De Coster ◽  
Virginia E Sturm ◽  
Joel H Kramer ◽  
...  

Abstract Deficits in emotion perception (the ability to infer others’ emotions accurately) can occur as a result of neurodegeneration. It remains unclear how different neurodegenerative diseases affect different forms of emotion perception. The present study compares performance on a dynamic tracking task of emotion perception (where participants track the changing valence of a film character’s emotions) with performance on an emotion category labeling task (where participants label specific emotions portrayed by film characters) across seven diagnostic groups (N = 178) including Alzheimer’s disease (AD), behavioral variant frontotemporal dementia (bvFTD), semantic variant primary progressive aphasia (svPPA), non-fluent variant primary progressive aphasia (nfvPPA), progressive supranuclear palsy (PSP), corticobasal syndrome and healthy controls. Consistent with hypotheses, compared to controls, the bvFTD group was impaired on both tasks. The svPPA group was impaired on the emotion labeling task, whereas the nfvPPA, PSP and AD groups were impaired on the dynamic tracking task. Smaller volumes in bilateral frontal and left insular regions were associated with worse labeling, whereas smaller volumes in bilateral medial frontal, temporal and right insular regions were associated with worse tracking. Findings suggest labeling and tracking facets of emotion perception are differentially affected across neurodegenerative diseases due to their unique neuroanatomical correlates.


2021 ◽  
Vol 17 (S6) ◽  
Author(s):  
Sheila Castro‐Suarez ◽  
Victor Osorio‐Marcatinco ◽  
Erik Alberto Guevara‐Silva ◽  
Cesar Caparo‐Zamalloa ◽  
Maria Meza‐Vega

2020 ◽  
Vol 35 ◽  
pp. 153331752092238
Author(s):  
Sunil Pradhan ◽  
Ruchika Tandon

Introduction: This study tried to find out type of lobar features found in patients with progressive supranuclear palsy (PSP) and whether they differ from those of frontotemporal dementia (FTD) as both of these are tauopathies. Methods: We studied lobar functions of 45 patients with PSP. Results: Five (11.1%) patients had no lobar feature; 11 (24.4%) had PSP-like features like apathy, frontal release signs, impaired motor Luria written sequences, and fist-edge-palm test; and 29 (64.4%) patients had FTD-like lobar features like disinhibition, poor naming, and word finding difficulty. Among features resembling FTD, behavioural variant type occurred in 31.1%, primary progressive aphasia type occurred in 58.6%, 3.4% patients had semantic dementia type features, and 6.9% were unclassified. Conclusions: Hence, patients with PSP with lobar features may fall in the middle of PSP-FTD spectrum with frontal lobe features typical of PSP (PSP-frontal like) and those with frontal lobe features resembling FTD (PSP-FTD complex) in between.


2016 ◽  
Vol 73 (6) ◽  
pp. 733 ◽  
Author(s):  
Miguel A. Santos-Santos ◽  
Maria Luisa Mandelli ◽  
Richard J. Binney ◽  
Jennifer Ogar ◽  
Stephen M. Wilson ◽  
...  

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