The Evolution of Alexia in Two Cases of Posterior Cortical Atrophy

Posterior cortical atrophy (PCA) is an uncommon presentation of Alzheimer's disease (AD), characterised by prevalent anatomo-functional involvement of posterior cortical areas. Accordingly, the main clinical features at onset are disorders of high-order visual processing, such as alexia and imp...

Full description

Saved in:
Bibliographic Details
Main Authors: Eleonora Catricalà, Pasquale A. Della Rosa, Paola Ortelli, Valeria Ginex, Alessandra Marcone, Daniela Perani, Stefano F. Cappa
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:Behavioural Neurology
Online Access:http://dx.doi.org/10.3233/BEN-2011-0334
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850179369404727296
author Eleonora Catricalà
Pasquale A. Della Rosa
Paola Ortelli
Valeria Ginex
Alessandra Marcone
Daniela Perani
Stefano F. Cappa
author_facet Eleonora Catricalà
Pasquale A. Della Rosa
Paola Ortelli
Valeria Ginex
Alessandra Marcone
Daniela Perani
Stefano F. Cappa
author_sort Eleonora Catricalà
collection DOAJ
description Posterior cortical atrophy (PCA) is an uncommon presentation of Alzheimer's disease (AD), characterised by prevalent anatomo-functional involvement of posterior cortical areas. Accordingly, the main clinical features at onset are disorders of high-order visual processing, such as alexia and impairments of visuo-spatial and visuo-constructional abilities. The clinical features in the early stages of disease are variable, and they have been suggested to stem from prevalent ventral or dorsal brain pathology, and/or asymmetric hemispheric involvement. With disease progression, these differences tend to blur with the increasing severity of neuropsychological dysfunction. We report two PCA patients showing different patterns of reading impairment (respectively, letter-by-letter reading and neglect dyslexia). A follow-up study suggested that the qualitative features of alexia remain distinctive with disease evolution. In addition, single photon emission tomography (SPECT) studies revealed different patterns of hypoperfusion, consistent with the alexia types. A careful reading assessment can provide important insights to the pattern of progression of the disease in patients with PCA up to the late stages of the pathology.
format Article
id doaj-art-9f398a83ec57428fb58b3f880df5f69d
institution OA Journals
issn 0953-4180
1875-8584
language English
publishDate 2011-01-01
publisher Wiley
record_format Article
series Behavioural Neurology
spelling doaj-art-9f398a83ec57428fb58b3f880df5f69d2025-08-20T02:18:32ZengWileyBehavioural Neurology0953-41801875-85842011-01-0124322923610.3233/BEN-2011-0334The Evolution of Alexia in Two Cases of Posterior Cortical AtrophyEleonora Catricalà0Pasquale A. Della Rosa1Paola Ortelli2Valeria Ginex3Alessandra Marcone4Daniela Perani5Stefano F. Cappa6Department of Psychology, Milano-Bicocca University, Milan, ItalyVita-Salute University and San Raffaele Scientific Institute, Milan, ItalyDepartment of Clinical Neurosciences, San Raffaele Turro Hospital, Milan, ItalyDepartment of Clinical Neurosciences, San Raffaele Turro Hospital, Milan, ItalyDepartment of Clinical Neurosciences, San Raffaele Turro Hospital, Milan, ItalyVita-Salute University and San Raffaele Scientific Institute, Milan, ItalyVita-Salute University and San Raffaele Scientific Institute, Milan, ItalyPosterior cortical atrophy (PCA) is an uncommon presentation of Alzheimer's disease (AD), characterised by prevalent anatomo-functional involvement of posterior cortical areas. Accordingly, the main clinical features at onset are disorders of high-order visual processing, such as alexia and impairments of visuo-spatial and visuo-constructional abilities. The clinical features in the early stages of disease are variable, and they have been suggested to stem from prevalent ventral or dorsal brain pathology, and/or asymmetric hemispheric involvement. With disease progression, these differences tend to blur with the increasing severity of neuropsychological dysfunction. We report two PCA patients showing different patterns of reading impairment (respectively, letter-by-letter reading and neglect dyslexia). A follow-up study suggested that the qualitative features of alexia remain distinctive with disease evolution. In addition, single photon emission tomography (SPECT) studies revealed different patterns of hypoperfusion, consistent with the alexia types. A careful reading assessment can provide important insights to the pattern of progression of the disease in patients with PCA up to the late stages of the pathology.http://dx.doi.org/10.3233/BEN-2011-0334
spellingShingle Eleonora Catricalà
Pasquale A. Della Rosa
Paola Ortelli
Valeria Ginex
Alessandra Marcone
Daniela Perani
Stefano F. Cappa
The Evolution of Alexia in Two Cases of Posterior Cortical Atrophy
Behavioural Neurology
title The Evolution of Alexia in Two Cases of Posterior Cortical Atrophy
title_full The Evolution of Alexia in Two Cases of Posterior Cortical Atrophy
title_fullStr The Evolution of Alexia in Two Cases of Posterior Cortical Atrophy
title_full_unstemmed The Evolution of Alexia in Two Cases of Posterior Cortical Atrophy
title_short The Evolution of Alexia in Two Cases of Posterior Cortical Atrophy
title_sort evolution of alexia in two cases of posterior cortical atrophy
url http://dx.doi.org/10.3233/BEN-2011-0334
work_keys_str_mv AT eleonoracatricala theevolutionofalexiaintwocasesofposteriorcorticalatrophy
AT pasqualeadellarosa theevolutionofalexiaintwocasesofposteriorcorticalatrophy
AT paolaortelli theevolutionofalexiaintwocasesofposteriorcorticalatrophy
AT valeriaginex theevolutionofalexiaintwocasesofposteriorcorticalatrophy
AT alessandramarcone theevolutionofalexiaintwocasesofposteriorcorticalatrophy
AT danielaperani theevolutionofalexiaintwocasesofposteriorcorticalatrophy
AT stefanofcappa theevolutionofalexiaintwocasesofposteriorcorticalatrophy
AT eleonoracatricala evolutionofalexiaintwocasesofposteriorcorticalatrophy
AT pasqualeadellarosa evolutionofalexiaintwocasesofposteriorcorticalatrophy
AT paolaortelli evolutionofalexiaintwocasesofposteriorcorticalatrophy
AT valeriaginex evolutionofalexiaintwocasesofposteriorcorticalatrophy
AT alessandramarcone evolutionofalexiaintwocasesofposteriorcorticalatrophy
AT danielaperani evolutionofalexiaintwocasesofposteriorcorticalatrophy
AT stefanofcappa evolutionofalexiaintwocasesofposteriorcorticalatrophy