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Clinical features and imaging findings in a case of Capgras syndrome

Capgras syndrome consists of the delusional belief that a person or persons have been replaced by doubles or impostors. It can occur in the context of both psychiatric and organic illness, and seems to be related to lesions of the bifrontal and right limbic and temporal regions. Indeed, magnetic res...

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Autores principales: Luca, Maria, Bordone, Andrea, Luca, Antonina, Patti, Andrea, Sortino, Giuseppe, Calandra, Carmela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742348/
https://www.ncbi.nlm.nih.gov/pubmed/23950650
http://dx.doi.org/10.2147/NDT.S47293
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author Luca, Maria
Bordone, Andrea
Luca, Antonina
Patti, Andrea
Sortino, Giuseppe
Calandra, Carmela
author_facet Luca, Maria
Bordone, Andrea
Luca, Antonina
Patti, Andrea
Sortino, Giuseppe
Calandra, Carmela
author_sort Luca, Maria
collection PubMed
description Capgras syndrome consists of the delusional belief that a person or persons have been replaced by doubles or impostors. It can occur in the context of both psychiatric and organic illness, and seems to be related to lesions of the bifrontal and right limbic and temporal regions. Indeed, magnetic resonance imaging has revealed brain lesions in patients suffering from Capgras syndrome. This case study reports the findings of a thorough diagnostic evaluation in a woman suffering from Capgras syndrome and presenting with the following clinical peculiarities: obsessive modality of presentation of the delusional ideation, intrusiveness of such ideation (that even disturbed her sleep), as well as a sense of alienation and utter disgust towards the double. These characteristics bring to mind the typical aspects of obsessive-compulsive disorder. Neuroanatomic investigation, through magnetic resonance imaging, performed on this patient showed alteration of the bilateral semioval centers, which are brain regions associated with the emotion of disgust and often show alterations in subjects suffering from obsessive-compulsive disorder. Hence, neuroimaging allows researchers to put forward the hypothesis of a common neuroanatomic basis for Capgras syndrome and obsessive-compulsive disorder, at least for cases in which the delusional ideation is associated with deep feelings of disgust and presents with a certain pervasiveness.
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spelling pubmed-37423482013-08-15 Clinical features and imaging findings in a case of Capgras syndrome Luca, Maria Bordone, Andrea Luca, Antonina Patti, Andrea Sortino, Giuseppe Calandra, Carmela Neuropsychiatr Dis Treat Case Report Capgras syndrome consists of the delusional belief that a person or persons have been replaced by doubles or impostors. It can occur in the context of both psychiatric and organic illness, and seems to be related to lesions of the bifrontal and right limbic and temporal regions. Indeed, magnetic resonance imaging has revealed brain lesions in patients suffering from Capgras syndrome. This case study reports the findings of a thorough diagnostic evaluation in a woman suffering from Capgras syndrome and presenting with the following clinical peculiarities: obsessive modality of presentation of the delusional ideation, intrusiveness of such ideation (that even disturbed her sleep), as well as a sense of alienation and utter disgust towards the double. These characteristics bring to mind the typical aspects of obsessive-compulsive disorder. Neuroanatomic investigation, through magnetic resonance imaging, performed on this patient showed alteration of the bilateral semioval centers, which are brain regions associated with the emotion of disgust and often show alterations in subjects suffering from obsessive-compulsive disorder. Hence, neuroimaging allows researchers to put forward the hypothesis of a common neuroanatomic basis for Capgras syndrome and obsessive-compulsive disorder, at least for cases in which the delusional ideation is associated with deep feelings of disgust and presents with a certain pervasiveness. Dove Medical Press 2013 2013-08-06 /pmc/articles/PMC3742348/ /pubmed/23950650 http://dx.doi.org/10.2147/NDT.S47293 Text en © 2013 Luca et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed.
spellingShingle Case Report
Luca, Maria
Bordone, Andrea
Luca, Antonina
Patti, Andrea
Sortino, Giuseppe
Calandra, Carmela
Clinical features and imaging findings in a case of Capgras syndrome
title Clinical features and imaging findings in a case of Capgras syndrome
title_full Clinical features and imaging findings in a case of Capgras syndrome
title_fullStr Clinical features and imaging findings in a case of Capgras syndrome
title_full_unstemmed Clinical features and imaging findings in a case of Capgras syndrome
title_short Clinical features and imaging findings in a case of Capgras syndrome
title_sort clinical features and imaging findings in a case of capgras syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742348/
https://www.ncbi.nlm.nih.gov/pubmed/23950650
http://dx.doi.org/10.2147/NDT.S47293
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