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Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria

BACKGROUND: Primary progressive aphasia (PPA) is a progressive language disorder associated with atrophy of the dominant language hemisphere, typically left. Current PPA criteria divide PPA into three variants: non-fluent (nfvPPA), semantic (svPPA) and logopenic (lvPPA). The classification of PPA in...

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Autores principales: Sitek, Emilia J., Narożańska, Ewa, Brockhuis, Bogna, Muraszko-Klaudel, Anna, Lass, Piotr, Harciarek, Michał, Sławek, Jarosław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207292/
https://www.ncbi.nlm.nih.gov/pubmed/25343001
http://dx.doi.org/10.12659/PJR.890320
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author Sitek, Emilia J.
Narożańska, Ewa
Brockhuis, Bogna
Muraszko-Klaudel, Anna
Lass, Piotr
Harciarek, Michał
Sławek, Jarosław
author_facet Sitek, Emilia J.
Narożańska, Ewa
Brockhuis, Bogna
Muraszko-Klaudel, Anna
Lass, Piotr
Harciarek, Michał
Sławek, Jarosław
author_sort Sitek, Emilia J.
collection PubMed
description BACKGROUND: Primary progressive aphasia (PPA) is a progressive language disorder associated with atrophy of the dominant language hemisphere, typically left. Current PPA criteria divide PPA into three variants: non-fluent (nfvPPA), semantic (svPPA) and logopenic (lvPPA). The classification of PPA into one of the three variants may be performed at 3 levels: I) clinical, II) imaging-supported, III) definite pathologic diagnosis. This paper aimed at assessing the feasibility of the imaging-supported diagnostics of PPA variants in the Polish clinical setting with access to magnetic resonance imaging (MRI) and single-photon emission computed tomography (SPECT) examinations. CASE REPORT: We present the clinical and neuroimaging data on 6 patients (4 women, 2 men) clinically diagnosed with PPA (3 with nfvPPA and 3 with lvPPA) in whom MRI and SPECT were performed in order to determine if imaging-supported diagnosis could be established in those cases. In 4 individuals (2 with nfvPPA and 2 with lvPPA) clinical diagnosis was supported by neuroimaging (SPECT, albeit not MRI), thus level II of PPA diagnosis could be established in those cases. MRI results were either inconsistent with the clinical diagnosis (Patients 1 and 2) or a mixed pattern of atrophy was observed (Patients 3–6). CONCLUSIONS: Imaging-supported diagnosis of PPA variant is more feasible with quantitative analysis of SPECT images than with purely qualitative visual analysis of MRI. Hypoperfusion abnormalities evidenced by SPECT are more variant-specific than patterns of atrophy.
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spelling pubmed-42072922014-10-23 Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria Sitek, Emilia J. Narożańska, Ewa Brockhuis, Bogna Muraszko-Klaudel, Anna Lass, Piotr Harciarek, Michał Sławek, Jarosław Pol J Radiol Case Report BACKGROUND: Primary progressive aphasia (PPA) is a progressive language disorder associated with atrophy of the dominant language hemisphere, typically left. Current PPA criteria divide PPA into three variants: non-fluent (nfvPPA), semantic (svPPA) and logopenic (lvPPA). The classification of PPA into one of the three variants may be performed at 3 levels: I) clinical, II) imaging-supported, III) definite pathologic diagnosis. This paper aimed at assessing the feasibility of the imaging-supported diagnostics of PPA variants in the Polish clinical setting with access to magnetic resonance imaging (MRI) and single-photon emission computed tomography (SPECT) examinations. CASE REPORT: We present the clinical and neuroimaging data on 6 patients (4 women, 2 men) clinically diagnosed with PPA (3 with nfvPPA and 3 with lvPPA) in whom MRI and SPECT were performed in order to determine if imaging-supported diagnosis could be established in those cases. In 4 individuals (2 with nfvPPA and 2 with lvPPA) clinical diagnosis was supported by neuroimaging (SPECT, albeit not MRI), thus level II of PPA diagnosis could be established in those cases. MRI results were either inconsistent with the clinical diagnosis (Patients 1 and 2) or a mixed pattern of atrophy was observed (Patients 3–6). CONCLUSIONS: Imaging-supported diagnosis of PPA variant is more feasible with quantitative analysis of SPECT images than with purely qualitative visual analysis of MRI. Hypoperfusion abnormalities evidenced by SPECT are more variant-specific than patterns of atrophy. International Scientific Literature, Inc. 2014-08-08 /pmc/articles/PMC4207292/ /pubmed/25343001 http://dx.doi.org/10.12659/PJR.890320 Text en © Pol J Radiol, 2014 This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited.
spellingShingle Case Report
Sitek, Emilia J.
Narożańska, Ewa
Brockhuis, Bogna
Muraszko-Klaudel, Anna
Lass, Piotr
Harciarek, Michał
Sławek, Jarosław
Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria
title Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria
title_full Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria
title_fullStr Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria
title_full_unstemmed Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria
title_short Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria
title_sort neuroimaging in the differential diagnosis of primary progressive aphasia – illustrative case series in the light of new diagnostic criteria
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207292/
https://www.ncbi.nlm.nih.gov/pubmed/25343001
http://dx.doi.org/10.12659/PJR.890320
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