A Case of Capgras Syndrome With Frontotemporal Dementia.


Journal

Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology
ISSN: 1543-3641
Titre abrégé: Cogn Behav Neurol
Pays: United States
ID NLM: 101167278

Informations de publication

Date de publication:
06 2019
Historique:
entrez: 18 6 2019
pubmed: 18 6 2019
medline: 14 1 2020
Statut: ppublish

Résumé

Capgras syndrome (CS), also called imposter syndrome, is a rare psychiatric condition that is characterized by the delusion that a family relative or close friend has been replaced by an identical imposter. Here, we describe a 69-year-old man with CS who presented to the Kemal Arikan Psychiatry Clinic with an ongoing belief that his wife had been replaced by an identical imposter. MRI showed selective anterior left temporal lobe atrophy. Quantitative EEG showed bilateral frontal and temporal slowing. Neuropsychological profiling identified a broad range of deficits in the areas of naming, executive function, and long-term memory. On the basis of these findings, we diagnosed frontotemporal dementia. This case demonstrates that CS can clinically accompany frontotemporal dementia.

Identifiants

pubmed: 31205125
doi: 10.1097/WNN.0000000000000191
pii: 00146965-201906000-00007
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

134-138

Auteurs

Baris Metin (B)

Department of Psychology, Uskudar University, Istanbul, Turkey.

Mehmet K Arikan (MK)

Department of Psychology, Uskudar University, Istanbul, Turkey.
Kemal Arikan Psychiatry Clinic, Istanbul, Turkey.

Sukriye A Kalem (SA)

Department of Neurology, School of Medicine, Istanbul University, Istanbul, Turkey.

Nevzat Tarhan (N)

Department of Psychology, Uskudar University, Istanbul, Turkey.

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Classifications MeSH