metricas
covid
Buscar en
Revista Colombiana de Psiquiatría (English Edition)
Toda la web
Inicio Revista Colombiana de Psiquiatría (English Edition) Factor structure of Cotard’s syndrome: Systematic review of case reports
Información de la revista
Vol. 49. Núm. 3.
Páginas 187-193 (julio - septiembre 2020)
Visitas
5782
Vol. 49. Núm. 3.
Páginas 187-193 (julio - septiembre 2020)
Review Article
Acceso a texto completo
Factor structure of Cotard’s syndrome: Systematic review of case reports
Estructura factorial del Síndrome de Cotard: revisión sistemática de reportes de caso
Visitas
5782
Jeff Huarcaya-Victoriaa,b,
Autor para correspondencia
jhuarcayav@usmp.pe

Corresponding author.
, José Bojórquez-De la Torrec, Jorge De la Cruz-Oréd
a Centro de Investigación en Salud Pública, Facultad de Medicina, Universidad de San Martín de Porres, Lima, Peru
b Departamento de Psiquiatría, Hospital Central de la Policía Nacional del Perú Luis N. Saenz, Lima, Peru
c Servicio de Enfermedades Psiquiátricas Agudas, Departamento de Hospitalización, Hospital Víctor Larco Herrera, Lima, Peru
d Departamento de Emergencia, Hospital Nacional Guillermo Almenara Irigoyen, Lima, Peru
Este artículo ha recibido
Información del artículo
Resumen
Texto completo
Bibliografía
Descargar PDF
Estadísticas
Figuras (2)
Tablas (2)
Table 1. Characteristics and diagnosis of 69 patients with Cotard’s syndrome reported between 2005 and 2018.
Table 2. Exploratory factor analysis of 14 symptoms.
Mostrar másMostrar menos
Abstract
Introduction

Cotard’s syndrome is a rare psychiatric condition. As a result, current information is mainly based on reports and case series.

Objective

To analyse the psychopathological characteristics and the grouping of the symptoms of the Cotard’s syndrome cases reported in the medical literature.

Methods

A systematic review of the literature of all reported cases of Cotard’s syndrome from 2005 to January 2018 was performed in the MEDLINE/PubMed database. Demographic variables and clinical characteristics of each case were collected. An exploratory factor analysis of the symptoms was performed.

Results

The search identified 86 articles, of which 69 were potentially relevant. After reviewing the full texts, 55 articles were selected for the systematic review, in which we found 69 cases. We found that the diagnosis of major depression (P < 0.001) and organic mental disorder (P = 0.004) were more frequent in the older group with Cotard’s syndrome. An exploratory factor analysis extracted 3 factors: psychotic depression, in which it includes patients with delusions of guilt (0.721), suicidal ideas (0.685), delusions of damnation (0.662), nihilistic delusions of the body (0.642), depression (0.522), and hypochondriacal delusions (0.535); delusive-hallucinatory, with patients who presented delusions of immortality (0.566), visual hallucinations (0.545) and nihilistic delusions of existence (0.451), and mixed, with patients who presented nihilistic delusions of concepts (0.702), anxiety (0.573), and auditory hallucinations (0.560).

Conclusions

The psychopathology of Cotard’s syndrome is more complex than the simple association with the delusion of being dead, since it encompasses a factorial structure organised into 3 factors.

Keywords:
Cotard’s syndrome
Nihilistic delusion
Depression
Psychopathology
Resumen
Introducción

El síndrome de Cotard es de rara aparición en la clínica psiquiátrica. Debido a esto, la información actual se basa principalmente en reportes y series de casos.

Objetivo

Analizar las características psicopatológicas y la agrupación de los síntomas de los casos de síndrome de Cotard reportados en la literatura médica.

Métodos

Se realizó en la base de datos MEDLINE/PubMed una búsqueda sistemática de la literatura de todos los casos de síndrome de Cotard reportados desde 2005 hasta enero de 2018. Se recolectaron variables demográficas y las características clínicas de cada caso. Se realizó un análisis factorial exploratorio de los síntomas.

Resultados

La búsqueda identificó 86 artículos, de los cuales 69 eran potencialmente relevantes. Luego de la revisión de los textos completos, se seleccionaron 55 artículos para la revisión sistemática, entre los cuales se hallaron 69 casos. En el grupo de más edad con síndrome de Cotard fueron más frecuentes los diagnósticos de depresión mayor (p < 0,001) y trastorno mental orgánico (p = 0,004). El análisis factorial exploratorio arrojó 3 factores: depresión psicótica, en la que se incluye a los pacientes con delirios de culpa (0,721), ideas suicidas (0,685), delirios de condena (0,662), delirio nihilista del cuerpo (0,642), depresión (0,522) y delirios hipocondriacos (0,535); delirante-alucinatorio, con pacientes que sufrían delirio de inmortalidad (0,566), alucinaciones visuales (0,545) y delirio nihilista de la existencia (0,451), y mixto, con pacientes que sufrían delirio nihilista de los conceptos (0,702), ansiedad (0,573) y alucinaciones auditivas (0,560).

Conclusiones

La psicopatología del síndrome de Cotard es más compleja que la simple asociación con el delirio de estar muerto, ya que abarca una estructura factorial organizada en 3 factores.

Palabras clave:
Síndrome de Cotard
Delirio nihilista
Depresión
Psicopatología
Texto completo
Introduction

Cotard’s syndrome is an uncommon psychiatric condition the main characteristic of which is nihilistic delusions, in which patients deny their own existence or the existence of parts of their bodies.1 It was first reported by Jules Cotard in 1880. Since then, the concept of this syndrome has passed through various vicissitudes.2

At present, Cotard's syndrome is usually considered a monothematic delusion.3 We believe this conceptualisation is erroneous, as it does not capture the original concept set out by Cotard, to whom this condition consisted of not only a belief that one is dead, but also anxiety, agitation, severe depression, suicidal behaviour and other delusional ideas (immortality, enormity, blame, damnation and hypochondria).2,4

In the medical literature, this syndrome is primarily explored through case reports; few studies have analysed case series. To our knowledge, the study that retrospectively analysed the largest number of cases was a study by Berrios et al.5, who reviewed 100 cases of patients with this syndrome reported between 1880 and 1993. They performed an exploratory analysis of psychopathological symptoms and found three factors: a) psychotic depression: anxiety, delusion of guilt, depression and auditory hallucinations; b) Cotard's syndrome type I: hypochondriacal delusions and nihilistic delusions relating to the body, concepts and existence; and c) Cotard's syndrome type II: anxiety, delusions of immortality, auditory hallucinations, nihilistic delusions relating to existence and suicidal behaviours. Cotard's syndrome type I would be the pure form of the syndrome, with nosological origins in delusions, not in affective disorders.5 This grouping has not been corroborated in other more recent cases. Subsequently, Consoli et al.6 supplemented the study by Berrios et al.5 by retrospectively studying another 38 cases reported between 1994 and 2005. We concur with the finding of Berrios et al.2 that suitable study of the neurological foundations of Cotard's syndrome requires mapping of its clinical characteristics and basic clinical correlations.

This systematic review was undertaken with the objective of analysing the psychopathological characteristics and groupings of symptoms in the cases of Cotard's syndrome reported in the medical literature since Consoli et al.6 conducted their study.

Methods

This systematic review was done in accordance with PRISMA statement guidelines.7 The MEDLINE database was searched via the PubMed interface for all cases of Cotard's syndrome reported between 1 January 2005 and 24 January 2018 using the following terms: (Cotard's Syndrome) OR (Cotard's delusion) OR (Cotard syndrome) OR (Cotard delusion) OR (nihilistic delusion). Articles written in English or Spanish were selected. The principal investigator (JHV) screened the eligible articles. First, the principal investigator reviewed the titles and abstracts of all the articles found, then, two investigators (JHV and JBD) reviewed the full text of the potentially relevant articles.

The methodology applied by Berrios et al. was used5 (with the authorisation of the authors). Each case was searched for the following variables: age; sex; anxiety; depression; nihilistic delusions (relating to concepts, relating to existence and relating to the body); hypochondriacal delusions; delusions of immortality, damnation and other delusions; auditory and visual hallucinations; catatonic symptoms; suicidal ideas and/or acts; and the diagnosis given by the authors of the case reports. Two investigators (JHV and JBD) extracted the data independently, then resolved any discrepancies by consensus.

An independent investigator (JDO) performed the statistical analysis. Percentages for each symptom and average ages were determined using descriptive statistical techniques. Differences in frequency of symptoms between males and females were explored using a two-proportion z-test. In addition, patients were split into age groups to analyse the frequency of the diagnoses using the proportion difference test.

An exploratory factor analysis was performed with symptoms as variables using the principal component analysis method, then adjusted using varimax rotation. The number of factors was determined using the criterion of an eigenvalue >1.

Results

The initial search yielded a total of 86 articles. After 17 articles that were neither case reports nor case series were excluded, 69 articles with reports of cases of Cotard's syndrome remained.8–74 These case reports were then reviewed and 14 more articles were excluded as the report could not be accessed63, was written in neither English nor Spanish64–72, lacked sufficient clinical data73,74 or had been included in the review by Consoli et al.6,75,76. By investigator agreement, 55 articles were included in this study8–62 (Fig. 1).

Fig. 1.

Flow chart of process of identifying and selecting articles.

(0.12MB).

The sample included 69 patients (31 males and 38 females), with a mean age of 51.33 ± 17.4 years. The most common diagnosis was major depression (46.4%) (Table 1). The most common symptoms were nihilistic delusion relating to existence (69.6%), nihilistic delusion relating to the body (62.3%) and depression (62.3%). Fig. 2 shows the frequency of the other symptoms.

Table 1.

Characteristics and diagnosis of 69 patients with Cotard’s syndrome reported between 2005 and 2018.

Age (years)  51,33 ± 17,4 (14−85) 
[0,1–2]Sex
Males  31 (44,9) 
Females  38 (55,1) 
[0,1–2]
[0,1–2]Diagnosis
Major depression  32 (46,4) 
Bipolar affective disorder  5 (7,2) 
Schizophrenia  7 (10,1) 
Organic mental illness  19 (27,5) 
[0,1–2]
Other  5 (7,2) 
Unspecified  1 (1,4) 

Values express n (%) or mean ± standard deviation.

Fig. 2.

Frequency of symptoms in 69 cases of Cotard's syndrome.

(0.13MB).

No significant differences were found between males and females in terms of symptom frequencies. Once the participants were divided into two age groups (≤25 and >25), the older group was found to have a higher rate of diagnosis of major depression (32 versus 2; p < 0.001) and organic mental illness (16 versus 3; p = 0.004). Within the group with a diagnosis of major depression, no significant differences in symptoms were found between males and females or between age groups. When only patients with a diagnosis of organic mental illness were considered, no relationships were found between symptoms and age group or between symptoms and sex.

Table 2 shows the exploratory factor analysis which was determined through a sediment graph. Variables were reduced by grouping them into three factors: 1, psychotic depression, with an eigenvalue of 3.112 and a variance of 22.23%, containing the symptoms of delusion of guilt (0.721), suicidal ideas (0.685), delusion of damnation (0.662), nihilistic delusion relating to the body (0.642), depression (0.522) and hypochondriacal delusion (0.535); 2, delusional/hallucinatory depression, with an eigenvalue of 1.88 and a variance of 13.48, containing the symptoms of delusion of immortality (0.566), visual hallucinations (0.545) and nihilistic delusion relation to existence (0.451); and 3, mixed, with an eigenvalue of 1.64 and a variance of 11.72, containing the symptoms of nihilistic delusion relating to concepts (0.702), anxiety (0.573) and auditory hallucinations (0.560). Varimax rotation did not improve the values for the symptoms in the components.

Table 2.

Exploratory factor analysis of 14 symptoms.

  [0,2–6]Factors
 
Anxiety  0,455  0,073  0,573  –0,398  0,036 
Depression  0,522  –0,377  –0,084  0,040  0,202 
Nihilistic delusion relating to concepts  0,161  –0,265  0,702  –0,343  0,303 
Nihilistic delusion relating to existence  –0,485  0,451  –0,129  –0,123  0,511 
Nihilistic delusion relating to the body  0,642  –0,351  –0,027  –0,050  –0,235 
Hypochondriacal delusion  0,535  0,249  –0,310  –0,364  –0,277 
Delusion of immortality  0,299  0,566  –0,170  0,205  0,403 
Delusion of guilt  0,721  0,098  0,079  0,078  0,313 
Delusion of damnation  0,662  0,336  –0,116  0,255  0,023 
Other delusions  –0,146  –0,277  0,384  0,454  0,233 
Auditory hallucination  0,142  0,469  0,560  0,214  –0,243 
Visual hallucination  0,108  0,545  0,345  0,345  –0,312 
Catatonic symptoms  0,322  –0,490  –0,081  0,572  0,038 
Suicidal thoughts/behaviours  0,685  0,069  –0,253  –0,132  0,151 

1: psychotic depression; 2: delusional/hallucinatory; 3: mixed.

Five factors extracted. Extraction method: principal factor analysis.

Discussion

Current knowledge of Cotard’s syndrome is based on case reports and case series with few patients. To our knowledge, this is the second retrospective study with the largest sample of patients with Cotard's syndrome.

The mean age of the patients was 51.33 years; this was similar to that reported in the study by Berrios et al.5. According to Séglas77, these patients’ psychopathology “manifests in adulthood, most often towards mid-life”.

The diagnoses of major depression and organic mental illness had a significant relationship with age (>25 years). This result contrasted with that reported by Consoli et al.6, who found that, in young patients with Cotard's syndrome (≤25 years of age), the diagnosis of bipolar affective disorder was more common and the risk of having this diagnosis was up to nine times higher (p < 0.0001).

Regarding symptom frequencies, nihilistic delusions were the most commonly identified symptoms. Cases may be of three types: a) nihilistic delusions relating to existence, in which patients deny their own somatic and/or spiritual existence; b) nihilistic delusions relating to the body, in which patients deny the existence of parts of their bodies, saying they do not have organs or are decomposed or “rotten on the inside”15; and c) nihilistic delusions relating to concepts, which affect metaphysical representations made by patients, who may state that nothing exists or deny other people's identities10. Interestingly, delusions of damnation, guilt and immortality were reported at a lower frequency than in cases from 1880 to 1993.5 This may be due to the fact that: a) in the course of the 20th century, Cotard’s syndrome, along with other clinical phenomena, underwent semantic degradation, such that at the present time there is a tendency to consider Cotard’s syndrome as a monothematic delusion, which is detrimental to preparing a more detailed pathophysiological report2,77,78; and b) general changes have occurred in the moral and religious culture of the Western world. Prior reviews did not take catatonic symptoms into account5,6; these were found in 23.2% of patients. Catatonic symptoms in Cotard's syndrome have classically been reported as uncommon. For some authors this would be due to the rarity of this association32, whereas for others these symptoms would be more common43. This could be explained, in part, by the fact that catatonic symptoms are often underdiagnosed for lack of investigation. In a worst-case scenario, this could lead to ineffective treatment resulting in serious complications for the patient’s life due to prolonged immobility and dehydration.

The exploratory factor analysis yielded three factors: psychotic depression, delusions/hallucinations and mixed. The psychotic depression factor included patients with depression, and the others may be psychopathological symptoms with said depression at their core. It could also be imagined that the delusional symptoms grouped in this factor have a relationship with the course of Cotard's syndrome (e.g. hypochondriacal delusions could develop into nihilistic delusions relating to the body and delusions of guilt, then delusions of damnation). The delusions/hallucinations factor features symptoms of depression, whereas the mixed factor features symptoms of anxiety, hallucinations and delusions. These results partly overlap with those reported by Berrios et al.5 Hence, Cotard’s syndrome may be thought to show factor coherence independent of time and space. These results have: a) certain implications for psychopathology, as there is a group of patients with Cotard’s syndrome whose psychopathology features not affective disorders, but instead phenomena of hallucinations/delusions — Saavedra79 noted that this may be seen in patients with schizophrenic psychosis, and that the psychopathology would be distorted by the phenomena of hallucinations and delusions thereof, and proposed the name “pseudo-Cotard's syndrome” for this form of presentation, as a variant of cenesthopathic schizophrenia — and b) certain implications for treatment, as patients with Cotard's syndrome with delusions/hallucinations probably do not show a suitable response to antidepressant treatment, such that an antipsychotic agent must be used5. Our clinical experience has indicated that taking this factor differentiation into consideration optimises treatment and treatment response.11,15

This study has significant limitations. Uncontrolled secondary sources were analysed, meaning that its findings were limited by the quality of the cases reported, which was not uniform. A systematic review of reported cases could not find any strong associations. However, if some hypotheses can be identified for future studies, psychiatrists should take into consideration the cases reported in the literature indicating that Cotard's syndrome is not exclusive to psychotic depression.

Conclusions

Cotard’s syndrome psychopathology is more complex than the mere association with the “delusion of being dead” that has marked the approach to the disease in recent decades. The cases reported between 2005 and 2018 showed a significant relationship between an age >25 years and a diagnosis of major depression or organic mental illness. The exploratory factor analysis of symptoms yielded three factors: psychotic depression, delusions/hallucinations and mixed. These had already been reported in another study with a different patient sample; hence, it is possible to consider these factors to exhibit factor coherence independent of space and time. These results would have implications for these patients’ psychopathology and treatment.

Conflicts of interest

The authors have no conflicts of interest to declare.

References
[1]
J. Cotard.
Del delusión hipocondriaco en una forma grave de melancolía ansiosa.
Delusións melancólicos: negación y enormidad, pp. 3-9
[2]
G.E. Berrios, R. Luque.
Cotard’s delusion or syndrome?: a conceptual history.
Compr Psychiatry, 36 (1995), pp. 218-223
[3]
M. Coltheart, R. Langdon, R. McKay.
Schizophrenia and monothematic delusions.
Schizopr Bull, 33 (2007), pp. 642-647
[4]
J. Cotard.
On hypochondriacal delusions in a severe form of anxious melancholia.
Hist Psychiatry, 10 (1999), pp. 274-278
[5]
G.E. Berrios, R. Luque.
Cotard’s syndrome: analysis of 100 cases.
Acta Psychiatr Scand, 91 (1995), pp. 185-188
[6]
A. Consoli, C. Soultanian, M.L. Tanguy, et al.
Cotard’s síndrome in adolescents and Young adults is associated with an increased risk of bipolar disorder.
Bipolar Disord, 9 (2007), pp. 665-668
[7]
A. Liberati, D.G. Altman, J. Tetzlaff, et al.
The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration.
PLoS Med, 6 (2009),
[8]
M. Torrisi, R. De Luca, P. Pollicino, et al.
Poststroke delusions: what about the neuroanatomical and neurofunctional basis?.
Appl Neuropsychol Adult, 19 (2018), pp. 1-5
[9]
P.P. Kuppili, R. Gupta, R.D. Pattanayak, S.K. Khandelwal.
Delusional denial of pregnancy: unique presentation of Cotard's syndrome in a patient with schizophrenia.
Asian J Psychiatr, 30 (2017), pp. 26-27
[10]
A. Sahoo, K.A. Josephs.
A neuropsychiatric analysis of the Cotard delusion.
J Neuropsychiatry Clin Neurosci, 30 (2018), pp. 58-65
[11]
J. Huarcaya-Victoria, M. Ledesma-Gastañadui, M. Huete-Cordova.
Cotard’s syndrome in a patient with schizophrenia: case report and review of the literature.
Case Rep Psychiatry, 2016 (2016),
[12]
L. Machado, L.E. Filho, L. Machado.
When the patient believes that the organs are destroyed: manifestation of Cotard’s syndrome.
Case Rep Med, 2016 (2016),
[13]
N. Bott, C. Keller, M. Kuppuswamy, D. Spelber, J. Zeier.
Cotard delusion in the context of schizophrenia: a case report and review of the literature.
Front Psychol, 7 (2016), pp. 1351
[14]
R. Oberndorfer, C. Schönauer, H. Eichbauer, K. Klaushofer, F. Friedrich.
Cotard syndrome in hypoactive delirium — a case report.
Psychiatr Danub, 29 (2017), pp. 500-502
[15]
J. Huarcaya-Victoria, M. Caqui.
Cotard’s Syndrome in a patient with major depressive disorder: case report.
Actas Esp Psiquiatr, 45 (2017), pp. 248-255
[16]
S. Solimine, S. Chan, S.K. Morihara.
Cotard syndrome: “I’m dead, so why do i need to eat?”.
Prim Care Companion CNS Disord, 18 (2016),
[17]
S. Riggs, T. Perry, J. Dowben, R. Burson.
Vive la France: three delusional disorders originally reported in the French medical literature.
Perspect Psychiatr Care, 53 (2017), pp. 5-9
[18]
S. Ogata, Y. Itohiya, Y. Sakamoto, et al.
Differential diagnosis of an elderly manic-depressive patient with depersonalization and other symptoms.
Case Rep Psychiatry, 2016 (2016),
[19]
N. Ozkan, O. Caliyurt.
Brain metabolism changes with 18F-fluorodeoxy-glucose-positron emission tomography in a patient with Cotard's syndrome.
Aust N Z J Psychiatry, 50 (2016), pp. 600-601
[20]
J. Maruo, Y. Haraguchi, H. Tateishi, et al.
Abnormal behaviours during pramipexole treatment for Cotard’s syndrome: a case report.
Psychogeriatrics, 16 (2016), pp. 283-286
[21]
P. Morgado, R. Ribeiro, J.J. Cerqueira.
Cotard Syndrome without depressive symptoms in a schizophrenic patient.
Case Rep Psychiatry, 2015 (2015),
[22]
D. De Berardis, M. Brucchi, N. Serroni, et al.
Cotard’s Syndrome after breast surgery successfully treated with aripiprazole augmentation of escitalopram: a case report.
Riv Psichiatr, 50 (2015), pp. 95-98
[23]
F. Sottile, L. Bonanno, G. Finzi, et al.
Cotard and Capgras syndrome after ischemic stroke.
J Stroke Cerebrovasc Dis, 24 (2015), pp. e103-e104
[24]
P. Solla, A. Cannas, G. Orofino, F. Marrosu.
Fluctuating Cotard syndrome in a patient with advanced Parkinson disease.
Neurologist, 19 (2015), pp. 70-72
[25]
F. Mouaffak, P. Lavaud, F. Hozer, et al.
Capgras’ and Cotard’s delusions associated with a particular pattern of cerebral activity in a severely depressed patient.
Prim Care Companion CNS Disord, 16 (2014),
[26]
S. Grover, J. Aneja, S. Mahajan, S. Varma.
Cotard’s syndrome: Two case reports and a brief review of literature.
J Neurosci Rural Pract, 5 Suppl 1 (2014), pp. S59-S62
[27]
S.S. Chatterjee, S. Mitra.
“I do not exist” — Cotard syndrome in insular cortex atrophy.
Biol Psychiatry, 77 (2015), pp. e52-e53
[28]
N.E. Parks, H.B. Rigby, G.J. Gubitz, J.J. Shankar, R.A. Purdy.
Dysmetropsia and Cotard’s syndrome due to migrainous infarction — or not?.
Cephalalgia, 34 (2014), pp. 717-720
[29]
A. Ghaffari Nejad, A. Mehdizadeh Zare Anari, F. Pouya.
Effect of cultural themes on forming Cotard’s syndrome: reporting a case of Cotard’s syndrome with depersonalization and out of body experience symptoms.
Iran J Psychiatry Behav Sci, 7 (2013), pp. 91-93
[30]
D.L. Perez, B.H. Fuchs, J. Epstein.
A case of cotard syndrome in a woman with a right subdural hemorrhage.
J Neuropsychiatry Clin Neurosci, 26 (2014), pp. E29-E30
[31]
Y. Kutsuzawa, Y. Kunii, I. Miura, et al.
High plasma monoamine metabolite levels in Cotard’s syndrome.
Psychiatry Clin Neurosci, 68 (2014), pp. 388
[32]
A. Basu, P. Singh, R. Gupta, S. Soni.
Cotard syndrome with catatonia: unique combination.
Indian J Psychol Med, 35 (2013), pp. 314-316
[33]
C. Weiss, J. Santander, R. Torres.
Catatonia, neuroleptic malignant syndrome, and cotard syndrome in a 22-year-old woman: a case report.
Case Rep Psychiatry, 2013 (2013),
[34]
L. Machado, A. Peregrino, S. Azoubel, H. Cerqueira, L.E. Lima Filho.
Cotard’s syndrome and major depression with psychotic symptoms.
Rev Bras Psiquiatr, 35 (2013), pp. 212
[35]
R. Lopes, I. Costa, R. Curral, M. Esteves, A. Roma-Torres.
The utility of intravenous clomipramine in a case of Cotard’s syndrome.
Rev Bras Psiquiatr, 35 (2013), pp. 212-213
[36]
A.C. Fonseca, E. Pinho, T. Melo, J.M. Ferro.
Cotard delusion after stroke.
Eur J Neurol, 20 (2013), pp. e98-e99
[37]
V. Charland-Verville, M.A. Bruno, M.A. Bahri, et al.
Brain dead yet mind alive: a positron emission tomography case study of brain metabolism in Cotard’s syndrome.
Cortex, 49 (2013), pp. 1997-1999
[38]
F. Mughal, S.B. Menezes.
Severe depression with Cotard’s phenomenon: treatment of a capacitated patient within the United Kingdom’s Mental Health Act 2007.
Ment Ill, 5 (2013), pp. e3
[39]
V. Sharma, D. Biswas.
Cotard’s syndrome in post-surgical patients.
J Neuropsychiatry Clin Neurosci, 24 (2012), pp. E42-E43
[40]
T. Kobayashi, K. Inoue, K. Shioda, S. Kato.
Effectiveness of electroconvulsive therapy for depression and Cotard's syndrome in a patient with frontotemporal lobe dementia.
Case Rep Psychiatry, 2012 (2012),
[41]
Y. Nishio, E. Mori.
Delusions of death in a patient with right hemisphere infarction.
Cogn Behav Neurol, 25 (2012), pp. 216-223
[42]
C.G. Huber, A. Agorastos.
We are all zombies anyway: aggression in Cotard’s syndrome.
J Neuropsychiatry Clin Neurosci, 24 (2012), pp. E21
[43]
P. Simpson, E. Kaul, D. Quinn.
Cotard’s syndrome with catatonia: a case presentation and discussion.
Psychosomatics., 54 (2013), pp. 196-199
[44]
M. Reich, B. Comet, E. Le Rhun, C. Ramirez.
Cotard’s syndrome with glioblastoma multiforme.
Palliat Support Care, 10 (2012), pp. 135-139
[45]
P. Alvarez, V.M. Puente, M.J. Blasco, P. Salgado, A. Merino, A. Bulbena.
Concurrent Koro and Cotard syndromes in a Spanish male patient with a psychotic depression and cerebrovascular disease.
Psychopathology, 45 (2012), pp. 126-129
[46]
M.F. Mendez, J. Ramírez-Bermúdez.
Cotard syndrome in semantic dementia.
Psychosomatics, 52 (2011), pp. 571-574
[47]
P.H. Chou, B.T. Lin, T.H. Lan, C.H. Chan.
Chronic Cotard’s syndrome: recovery from 2 years’ bed-ridden status.
Psychiatry Clin Neurosci, 65 (2011), pp. 301
[48]
J. Ramirez-Bermudez, L.C. Aguilar-Venegas, D. Crail-Melendez, et al.
Cotard syndrome in neurological and psychiatric patients.
J Neuropsychiatry Clin Neurosci, 22 (2010), pp. 409-416
[49]
D. De Berardis, N. Serroni, D. Campanella, V. Marasco, F.S. Moschetta, M. Di Giannantonio.
A case of Cotard’s Syndrome successfully treated with aripiprazole monotherapy.
Prog Neuropsychopharmacol Biol Psychiatry., 34 (2010), pp. 1347-1348
[50]
S. Grover, R. Shah, A. Ghosh.
Electroconvulsive therapy for lycanthropy and Cotard syndrome: a case report.
[51]
T. Takahashi, M. Nibuya, S. Nomura.
Delusion of Cotard’s syndrome successfully treated with a dopamine agonist.
J Neuropsychiatry Clin Neurosci., 22 (2010), pp. E27
[52]
V. Altinyazar, N. Kiylioglu, G. Salkin.
Anorexia nervosa and Wernicke Korsakoff’s syndrome: atypical presentation by acute psychosis.
Int J Eat Disord, 43 (2010), pp. 766-769
[53]
G. Fàzzari, O. Benzoni, A. Sangaletti, et al.
Improvement of cognition in a patient with Cotard’s delusions and frontotemporal atrophy receiving electroconvulsive therapy (ECT) for depression.
Int Psychogeriatr, 21 (2009), pp. 600-603
[54]
J.H. Chan, C.H. Chen, D. Robson, H.K. Tan.
Case report: effective treatment of Cotard’s syndrome: quetiapine in combination with venlafaxine.
Psychiatry Clin Neurosci, 63 (2009), pp. 125-126
[55]
A. Ruminjo, B. Mekinulov.
A case report of Cotard’s syndrome.
Psychiatry (Edgmont), 5 (2008), pp. 28-29
[56]
Z.A. Wani, A.W. Khan, A.A. Baba, H.A. Khan, Q.U. Wani, R. Taploo.
Cotard’s syndrome and delayed diagnosis in Kashmir, India.
Int J Ment Health Syst, 2 (2008), pp. 1
[57]
A. Ghaffari-Nejad, M. Kerdegari, H. Reihani-Kermani.
Self-mutilation of the nose in a schizophrenic patient with Cotard syndrome.
Arch Iran Med, 10 (2007), pp. 540-542
[58]
J.H. Montgomery, D. Vasu.
The use of electroconvulsive therapy in atypical psychotic presentations: a case review.
Psychiatry (Edgmont), 4 (2007), pp. 30-39
[59]
R. McKay, L. Cipolotti.
Attributional style in a case of Cotard delusion.
Conscious Cogn, 16 (2007), pp. 349-359
[60]
J.E. Walloch, C. Klauwer, M. Lanczik, I.F. Brockington, J. Kornhuber.
Delusional denial of pregnancy as a special form of Cotard’s syndrome: case report and review of the literature.
Psychopathology, 40 (2007), pp. 61-64
[61]
D.N. Mendhekar, N. Gupta.
Recurrent postictal depression with Cotard delusion.
Indian J Pediatr, 72 (2005), pp. 529-531
[62]
T. Krisanaprakornkit, S. Paholpak, K. Tassaniyom, V. Pimpanit.
Transcranial magnetic stimulation for treatment resistant depression: six case reports and review.
J Med Assoc Thai, 93 (2010), pp. 580-586
[63]
K. Lally, N. Ibrahim, M. Kelly, G. Gulati.
Brief psychotic episode in a patient with chromosome 2q37 microdeletion syndrome.
[64]
N.P. Moschopoulos, S. Kaprinis, J. Nimatoudis.
Cotard’s syndrome: case report and a brief review of literature.
Psychiatriki, 27 (2016), pp. 296-302
[65]
T. Mamaeva, D.S. Christensen, C.T. Nielsen.
Electroconvulsive therapy is efficient in treating Cotard’s syndrome.
Ugeskr Laeger, (2016), pp. 178
[66]
T. Fuke, T. Takahashi, Y. Yamada, M. Miyashita, N. Amano, M. Matsushita.
Cotard’s syndrome in three patients with schizophrenia—pathology of involutional and senile-onset endogenous psychosis.
Seishin Shinkeigaku Zasshi, 117 (2015), pp. 257-268
[67]
T. Stompe, H. Schanda.
The Cotard syndrome in schizophrenic disorders.
Neuropsychiatr, 27 (2013), pp. 38-46
[68]
P.L. Bandinelli, M. Trevisi, G.D. Kotzalidis, G. Manfredi, C. Rapinesi, G. Ducci.
Chronic Koro-like Syndrome (KLS) in recurrent depressive disorder as a variant of Cotard’s delusion in an italian male patient. A case report and historical review.
Riv Psichiatr, 46 (2011), pp. 220-226
[69]
J. Bjerre, C. Fontenay.
Ketamine in melancholic depression.
Ugeskr Laeger, 172 (2010), pp. 460-461
[70]
M. Grzywa, M. Kloc-Rojek, A. Zaborska.
Severe depressive episode with psychotic symptoms on the basis of hypothyroidism.
Pol Merkur Lekarski, 27 (2009), pp. 397-399
[71]
Y. Madani, B.G. Sabbe.
Cotard’s syndrome. Different treatment strategies according to subclassification.
Tijdschr Psychiatr, 49 (2007), pp. 49-53
[72]
R. Kozian.
Brief case report. Duloxetine in Cotard syndrome.
Psychiatr Prax, 32 (2005), pp. 412-413
[73]
J.J. Gan, A. Lin, M.S. Samimi, M.F. Mendez.
Somatic symptom disorder in semantic dementia: the role of alexisomia.
Psychosomatics, 57 (2016), pp. 598-604
[74]
P. Muñoz, M. Valerio, J. Palomo, et al.
Infectious and non-infectious neurologic complications in heart transplant recipients.
Medicine (Baltimore), 89 (2010), pp. 166-175
[75]
R.C. Christensen.
Dead men walking. Reflections on Cotard’s syndrome and homelessness.
Pharos Alpha Omega Alpha Honor Med Soc, 68 (2005), pp. 33-34
[76]
A.G. Nejad, K. Toofani.
Co-existence of lycanthropy and Cotard’s syndrome in a single case.
Acta Psychiatr Scand, 111 (2005), pp. 250-252
[77]
J. Séglas.
El delusión de negación. Semiología y diagnóstico.
Delusións melancólicos: Negación y Enormidad, pp. 63-197
[78]
N. Andreasen.
DSM and the death of phenomenology in America: an example of unintended consequences.
Schizoph Bull, 33 (2007), pp. 108-112
[79]
V. Saavedra.
El síndrome de Cotard. Consideraciones psicopatológicas y nosográficas.
Rev Neuropsiquiatr, 31 (1968), pp. 145-174

Please cite this article as: Huarcaya-Victoria J, la Torre JB-D, De la Cruz-Oré J. Estructura factorial del Síndrome de Cotard: revisión sistemática de reportes de caso. Rev Colomb Psiquiat. 2020;49:187–193.

Copyright © 2018. Asociación Colombiana de Psiquiatría
Descargar PDF
Opciones de artículo
Quizás le interese:
10.1016/j.rcpeng.2024.10.006
No mostrar más