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A review of the phenomenology and cognitive neuropsychological origins of the Capgras syndrome.

In this article the epidemiology, aetiology, neuroanatomy and neuropsychology of the Capgras syndrome (CS) are reviewed in detail. CS is characterized by the delusional belief that one or a few highly familiar people have been replaced by impostors who are physically very similar to the original/s. The patient acknowledges that the double and known person look alike, but maintains the belief that the significant person, in psychological terms, is absent. CS is relatively rare, occurring predominantly in the context of schizophrenia, and was traditionally considered to have its origins in psychodynamic conflict. More recently, however, it has been estimated that between 25 and 40% of cases are associated with organic disorders, which include dementia, head trauma, epilepsy and cerebrovascular disease. Neuroimaging evidence suggests a link between CS and right hemisphere abnormalities, particularly in the frontal and temporal regions. Neuropsychological research has provided empirical support for these findings, by consistently reporting the presence of impairments in facial processing--an established right hemisphere function. It is likely that the study of this symptom will lead to a greater understanding of the neurological basis of psychotic experiences and may provide a paradigm for how the psychoses should be investigated.

Capgras Syndrome↗

[Capgras' syndrome].

We present 3 cases of Capgras' syndrome-a delusional disorder in which the patient believes that 1 (or more) of his acquaintances has been replaced by an imposter who appears as a double. 2 were schizophrenics and 1 had depression with psychotic features. This syndrome is rare in our practice, but we do not know if this is due to lack of awareness of the condition, or to the possibility that it is a culture-related syndrome. We suggest that although the syndrome has lost some of it's significance, it is still worth making the diagnosis because of the medical and psychological implications this condition carries.

Adult↗

[Capgras syndrome: evolution of the hypotheses].

OBJECTIVE: to trace the evolution of hypotheses concerning Capgras' syndrome. METHODS: The data consist of slightly over 60 studies published between 1866 and 1994 which were selected in terms of their innovative nature and relevance to the clinical description of the syndrome and to psychodynamic, neurological and neuropsychological interpretations. RESULTS: Two partially overlapping major stages can be identified in the evolution of hypotheses regarding the mechanisms of the syndrome. The 1st, beginning in 1923, is characterized by the predominance of psychodynamic interpretations. The 2nd, resulting from the observation of organic dysfunctions in a high percentage of cases, is distinguished by the advent of neurological interpretations, and by a few mixed hypotheses. CONCLUSIONS: Overall, this review highlights the broad diversity of viewpoints concerning the syndrome. It will be used as a basis for the following study, which is designed to show that it is possible to test each of the viewpoints experimentally.

Capgras Syndrome↗

Capgras syndrome--the many avenues to delusional misinterpretation.

The case of a 47 year old woman with Capgras' Syndrome is presented. Despite her misinterpretation of acoustic and visual clues, multiple investigations and extensive neuropsychological testing failed to implicate an organic basis upon which to explain her delusional belief. The authors conclude that single explanatory hypotheses--psychological or neurological--may preclude an appreciation for the heterogeneity of the syndrome.

Capgras Syndrome↗

Prevalence and correlates of Capgras syndrome in Alzheimer's disease.

OBJECTIVES: This study examined the prevalence and clinical correlates of Capgras syndrome (CS) in Alzheimer's disease. DESIGN: Cross-sectional study of elderly patients evaluated at an outpatient memory disorders clinic classified according to the presence or absence of CS. SUBJECTS: One hundred and fifty-one consecutive patients diagnosed with probable (N=110) or possible (N=48) Alzheimer's disease (AD) utilizing NINCDS-ADRDA diagnostic criteria. MATERIALS: The Behavioral Pathology in Alzheimer's Disease Rating Scale (BEHAVE-AD), Mini-Mental State Examination (MMSE) and Blessed Dementia Scale (BDS). RESULTS: CS was observed in 10% of the sample (N=16). Associated factors included other delusions, lower MMSE scores and higher BDS scores. The relation between CS and both cognitive and functional status remained significant after controlling for other delusions. CONCLUSION: CS was prevalent in approximately 10% of our community-dwelling AD sample. This syndrome was more common at the later stages of the illness and showed relations with increased functional impairment and other psychotic symptomatology.

Aged↗

Capgras syndrome.

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Adolescent↗

Capgras syndrome in a patient with myxedema.

The authors describe what may be the first reported case of Capgras syndrome associate with, or precipitated by, myxedema. The patient's mental status dramatically returned to normal with gradual thyroid replacement. The authors suggest that tests for organicity be done routinely on patients manifesting Capgras features.

Aged↗

Capgras syndrome heralding the development of dementia.

Delusional misidentification of people otherwise well known, referred to as the Capgras syndrome, has been described in both functional and organic conditions. Evidence is accruing to suggest that it would always be prudent to search vigorously for an organic aetiology.

Aged↗

[Case with probable dementia with Lewy bodies, who shows reduplicative paramnesia and Capgras syndrome].

We report a case of probable dementia with Lewy bodies (DLB), showing reduplicative paramnesia (RP) and Capgras syndrome (CS). The patient, a right-handed 60 year-old male, began to show progressive dementia. At the age of 65, he showed fluctuating cognitive impairment and recurrent visual hallucinations. His SPECT demonstrated hypoperfusion not in the medial temporal cortices, but in the parieto-occipital lobes, where the right hemisphere was dominantly hypoperfused. He was diagnosed with probable DLB. In addition to recurrent visual hallucinations, he showed a sense of self- (or others) transfiguration, consciousness of something non-existent (Leibhaftige Bewusstheit; Jaspers, K.), and fluctuating visuo-spacial impairment. At the age of 67, he gradually complained of his duplicative wives "sosie". Finally he went so far as to talk about a nameless phantom boarder. We considered that RP and CS of this case comprised a sense of self-(or others) transfiguration, misidentification of important persons and places, and productive symptoms such as consciousness of something non-existent (Leibhaftige Bewusstheit) and visual hallucinations. The above mentioned symptoms might be originated not only from the disturbance of visuospacial recognition, which involves the limbic system (especially amygdala), medial frontal cortex, and right hemisphere of the brain, but also from the disturbance of recursive consciousness, due to diffusely damaged brain regions with Lewy body pathology. (Authors' abstract)

Aged↗

An unusual case of Capgras syndrome: the psychiatric ward as a stage.

A 31-year-old male psychiatric patient presented with an unusual multifaceted delusion of misidentification including Capgras syndrome, in which people in the immediate environment, the other patients and hospital staff, were seen as hired actors in a stage production. The genesis and reinforcement of his delusional thinking appears to be the results of psychological, organic, and ecological factors.

Adult↗

Capgras syndrome: a review of the neurophysiological correlates and presenting clinical features in cases involving physical violence.

OBJECTIVE: Acts of violence have been frequently reported in cases of Capgras syndrome (CS), a misidentification syndrome characterized by the delusional belief that imposters have replaced people familiar to the individual. CS has been observed in many neuropsychiatric and organic disorders, and neuroimaging studies indicate an association between CS and right hemisphere abnormalities. However, CS has received limited attention from a forensic psychiatric perspective. We propose that elucidating demographic and clinical features noted in cases of violence secondary to CS may highlight important factors in the progression of CS to violence. METHOD: We review the neurophysiological correlates and clinical factors observed in CS and present characteristics of a series of cases that demonstrate the potential of CS patients for severe physical violence toward the misidentified person. RESULTS: For patients with CS involving assault, we present and discuss commonly reported demographic and clinical features that may contribute to an increased risk for violence. CONCLUSIONS: An understanding of the presenting clinical features of CS resulting in aggressive acts may assist clinicians to assess the potential for violence in these patients.

Brain↗

A rare case of Capgras syndrome observed in wake-amine induced psychosis.

An adolescent girl showed the apparent Capgras syndrome in the course of wake-amine induced psychosis. The patient, then 18, committed homicide in close connection with the syndrome and also with the distorted judgment due to personality immaturity. As far as the syndrome was concerned, the extension was so extreme that it involved her neighbors and even her dwelling city. The detailed case history was reported along with a discussion about the psychodynamism.

Adolescent↗

[Capgras' syndrome with right frontal meningioma].

We present a 43-year-old woman with a right frontal parasagittal meningioma of the brain who developed the delusion that her husband and children had been replaced by doubles (look-alikes). This type of delusion is typical for Capgras' syndrome. After removal of the tumor the delusion disappeared. The majority of such patients are diagnosed as paranoid schizophrenia. However, in the past decade there has been an increasing number of cases in which the etiology is suspected of being organic, involving mainly the right hemisphere. The case presented is unique because it is the first with meningioma as a possible pathogenic factor in the syndrome, as evidenced by the cessation of the delusion when the tumor was removed.

Adult↗

Capgras syndrome and functional psychosis in 2 survivors of torture.

Functional psychosis has only rarely been described in context with extreme stressors, most studies focusing singularly on posttraumatic stress disorder symptoms. We report for the first time the case histories of 2 patients suffering from Capgras syndrome along with schizoaffective disorder and posttraumatic stress disorder after prior experience of prolonged torture. Interaction of personal life experience and psychiatric disorder are proposed as factors resulting in persistent changes in perception and affect.

Adult↗