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Journal articles on the topic 'Syndrome de Cotard'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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1

Revilla, Joshep, Stephanie Aliaga, and Antonio Lozano-Vargas. "Cotard and Capgras Syndrome in a Patient with Treatment-Resistant Schizophrenia." Case Reports in Psychiatry 2021 (January 23, 2021): 1–3. http://dx.doi.org/10.1155/2021/6652336.

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The presentation of both Cotard and Capgras syndromes is uncommon in schizophrenia. We present a case of a 23-year-old male with the diagnosis of schizophrenia with Cotard syndrome who later developed Capgras syndrome. By persisting significant symptoms despite the use of two antipsychotics, he was given the diagnosis of treatment-resistant schizophrenia, and his symptoms improved with clozapine. This is one of the few cases of Cotard and Capgras syndromes in a patient with schizophrenia.

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2

Huarcaya-Victoria, Jeff, Mario Ledesma-Gastañadui, and Maria Huete-Cordova. "Cotard’s Syndrome in a Patient with Schizophrenia: Case Report and Review of the Literature." Case Reports in Psychiatry 2016 (2016): 1–7. http://dx.doi.org/10.1155/2016/6968409.

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Jules Cotard described, in 1880, the case of a patient characterized by delusions of negation, immortality, and guilt as well as melancholic anxiety among other clinical features. Later this constellation of symptoms was given the eponym Cotard’s syndrome, going through a series of theoretical vicissitudes, considering itself currently as just the presence of nihilistic delusions. The presentation of the complete clinical features described by Cotard is a rare occurrence, especially in the context of schizophrenia. Here we present the case of a 50-year-old male patient with schizophrenia who d

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3

Morgado, Pedro, Ricardo Ribeiro, and João J. Cerqueira. "Cotard Syndrome without Depressive Symptoms in a Schizophrenic Patient." Case Reports in Psychiatry 2015 (2015): 1–3. http://dx.doi.org/10.1155/2015/643191.

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Introduction. Cotard syndrome is a rare condition characterized by nihilistic delusions concerning body or life that can be found in several neuropsychiatry conditions. It is typically associated with depressive symptoms.Method. We present a case of Cotard syndrome without depressive symptoms in the context of known paranoid schizophrenia. A literature review of Cotard syndrome in schizophrenia was performed.Results. Although there are few descriptions of this syndrome in schizophrenia, patients usually present depressive mood and psychomotor retardation, features not seen in our patient. Loss

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4

Cacho, Jorge. "Le syndrome de Cotard." Journal français de psychiatrie 35, no. 4 (2009): 10. http://dx.doi.org/10.3917/jfp.035.0010.

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5

Samico, A., J. Perestrelo, and Â. Venâncio. "Cotard syndrome: Pathology review." European Psychiatry 41, S1 (2017): S746. http://dx.doi.org/10.1016/j.eurpsy.2017.01.1382.

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IntroductionCotard syndrome (CS) is a rare neuropsychiatric condition characterized by nihilistic delusions, which may range from negation of existence of parts of the body to delusion of being dead or negation of self-existence, and it requires an urgent and appropriate therapy.ObjectivesOur objective is to highlight the importance of CS, reinforcing that medical professionals should be aware of this pathology to prompt clinical description, diagnostic and treatment.AimsThe aim of this presentation is to alert psychiatrists to this remaining syndrome.MethodsReview of phenomenological and theo

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MACHADO, LILIANE, and LEONARDO MACHADO. "COTARD SYNDROME: THE DISEASE OF IMMORTALITY." Revista Debates em Psiquiatria Ano 5 (October 1, 2015): 34–37. http://dx.doi.org/10.25118/2236-918x-5-5-6.

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A síndrome de Cotard é uma condição rara caracterizada por melancolia ansiosa, delírios de não existência relativos ao próprio corpo e delírios de imortalidade. Neste artigo, relatamos o caso de um paciente do sexo masculino, com 66 anos de idade, com síndrome de Cotard refratária a psicofármacos e tratado com eletroconvulsoterapia. São discutidas algumas peculiaridades do manejo diagnóstico e terapêutico desta condição.

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7

Mendez, Mario F., and Jesús Ramírez-Bermúdez. "Cotard Syndrome in Semantic Dementia." Psychosomatics 52, no. 6 (2011): 571–74. http://dx.doi.org/10.1016/j.psym.2011.06.004.

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8

Basu, Aniruddha, Priti Singh, Rajiv Gupta, and Sandeep Soni. "Cotard Syndrome with Catatonia: Unique Combination." Indian Journal of Psychological Medicine 35, no. 3 (2013): 314–16. http://dx.doi.org/10.4103/0253-7176.119490.

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9

Gorina, E. A. "Cotard syndrome. History and modern view." V.M. BEKHTEREV REVIEW OF PSYCHIATRY AND MEDICAL PSYCHOLOGY, no. 2 (July 11, 2019): 13–19. http://dx.doi.org/10.31363/2313-7053-2019-2-13-19.

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In this review, we have collected the latest data on Kotar syndrome. The question of its nosological affiliation is considered, etiological theories and epidemiological indicators are presented. The options for the development of the clinical picture are described, data on the results of neuroimaging diagnostic studies are presented.

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10

Cercos López, A., M. C. Cancino Botello, V. Chavarria Romero, and G. Sugranyes Ernest. "Cotard syndrome in a young man?" European Psychiatry 33, S1 (2016): S348. http://dx.doi.org/10.1016/j.eurpsy.2016.01.1232.

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IntroductionAnti-NMDA encephalitis normally appears as a characteristic syndrome with typical symptoms that undergoes with multiphase evolution. However, it sometimes develops atypical symptoms so we must perform a careful differential diagnosis.ObjectivesTo conduct a current review of detection and management of anti-NMDAr encephalitis, and psychiatric manifestations.MethodSystematic review of the literature in English (PubMed), with the following keywords: “Autoimmune encephalitis”, “psychosis”, and “NMDA receptor”.ResultsWe present the case of a 15-year-old boy referred to evaluation for a

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11

Gennaro, Rocco Joseph. "Cotard syndrome, self-awareness, and I-concepts." Philosophy and the Mind Sciences 1, no. I (2020): 1–20. http://dx.doi.org/10.33735/phimisci.2020.i.41.

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Various psychopathologies of self-awareness, such as somatoparaphrenia and thought insertion in schizophrenia, might seem to threaten the viability of the higher-order thought (HOT) theory of consciousness since it requires a HOT about one’s own mental state to accompany every conscious state. The HOT theory of consciousness says that what makes a mental state a conscious mental state is that there is a HOT to the effect that “I am in mental state M.” I have argued in previous work that a HOT theorist can adequately respond to this concern with respect to somatoparaphrenia and thought insertio

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12

Machado, Leonardo, Luiz Evandro de Lima Filho, and Liliane Machado. "When the Patient Believes That the Organs Are Destroyed: Manifestation of Cotard’s Syndrome." Case Reports in Medicine 2016 (2016): 1–3. http://dx.doi.org/10.1155/2016/5101357.

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Cotard’s Syndrome (CS) is a rare clinical event described for the first time in 1880 by the neurologist and psychiatrist Jules Cotard and characterized by negation delusions (or nihilists). Immortality and hypochondriac delusions are also typical. Nowadays, it is known that CS can be associated with many neuropsychiatric conditions. In this article, we describe the case of a patient that believed not having more organs and having the body deformed and whose CS was associated with a bigger depressive disorder. Although the electroconvulsive therapy is the most described treatment modality in th

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13

Sottile, Fabrizio, Lilla Bonanno, Giuseppina Finzi, et al. "Cotard and Capgras Syndrome after Ischemic Stroke." Journal of Stroke and Cerebrovascular Diseases 24, no. 4 (2015): e103-e104. http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2015.01.001.

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14

Steno Hansen, Elsebet, and Tom G. Bolwig. "Cotard syndrome: An important manifestation of melancholia." Nordic Journal of Psychiatry 52, no. 6 (1998): 459–64. http://dx.doi.org/10.1080/08039489850139238.

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15

Cipriani, Gabriele, Angelo Nuti, Sabrina Danti, Lucia Picchi, and Mario Di Fiorino. "‘I am dead’: Cotard syndrome and dementia." International Journal of Psychiatry in Clinical Practice 23, no. 2 (2019): 149–56. http://dx.doi.org/10.1080/13651501.2018.1529248.

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16

Ramirez-Bermudez, Jesus, Luis C. Aguilar-Venegas, Daniel Crail-Melendez, Mariana Espinola-Nadurille, Francisco Nente, and Mario F. Mendez. "Cotard Syndrome in Neurological and Psychiatric Patients." Journal of Neuropsychiatry and Clinical Neurosciences 22, no. 4 (2010): 409–16. http://dx.doi.org/10.1176/jnp.2010.22.4.409.

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17

Grover, Sandeep, Ruchita Shah, and Abhishek Ghosh. "Electroconvulsive Therapy for Lycanthropy and Cotard Syndrome." Journal of ECT 26, no. 4 (2010): 280–81. http://dx.doi.org/10.1097/yct.0b013e3181e63357.

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18

Arce Ross, German. "Syndrome de Cotard et fuite des idées." L'Évolution Psychiatrique 70, no. 1 (2005): 161–76. http://dx.doi.org/10.1016/j.evopsy.2004.06.005.

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19

Butler, Peter V. "Diurnal Variation in Cotard's Syndrome (Copresent with Capgras Delusion) Following Traumatic Brain Injury." Australian & New Zealand Journal of Psychiatry 34, no. 4 (2000): 684–87. http://dx.doi.org/10.1080/j.1440-1614.2000.00758.x.

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Objective: The aim of this paper is to document regular nocturnal intensification of delusional nihilistic and persecutory ideas (Cotard delusion) linked with extreme depersonalisation and hypervivid dreaming. Clinical Picture: A 17-year-old man presented with Cotard and Capgras delusions after sustaining multiple cognitive impairments secondary to traumatic brain injury. Treatment and outcome: Delusional ideation fully resolved within 14 days of commencement of olanzapine 5 mg daily. Conclusion: This patient's experience of perceptual abnormalities and impairments in meta-abilities related to

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20

Oberndorfer, Raimund, Christoph Schonauer, Hans Eichbauer, Klaus Klaushofer, and Fabian Friedrich. "COTARD SYNDROME IN HYPOACTIVE DELIRIUM – A CASE REPORT." Psychiatria Danubina 29, no. 4 (2017): 500–502. http://dx.doi.org/10.24869/psyd.2017.500.

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21

Abellán Miralles, Inmaculada, Gloria González Caballero, Belén Piñol Ferrer, Concepción Morales Espinosa, Mar Ferrer Navajas, and María Josefa Sáenz Sanjuán. "Cotard syndrome in degenerative dementia. Report of three patients." Alzheimer. Realidades e investigación en demencia, no. 56 (January 1, 2014): 30–36. http://dx.doi.org/10.5538/1137-1242.2014.56.30.

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22

Factor, Stewart A., and Eric S. Molho. "Threatening Auditory Hallucinations and Cotard Syndrome in Parkinson Disease." Clinical Neuropharmacology 27, no. 5 (2004): 205–7. http://dx.doi.org/10.1097/01.wnf.0000144040.20600.c1.

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23

Shaan, Faisal, Abid Rizvi, and Gaurav Sharma. "Cotard syndrome in Tumefactive Multiple Sclerosis- A case report." Asian Journal of Psychiatry 34 (April 2018): 57–58. http://dx.doi.org/10.1016/j.ajp.2018.04.002.

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24

Pitta, Giovanni, Marcelo O’Higgins, Noelia Ruiz-Díaz, et al. "Síndrome de Cotard en una paciente con lupus eritematoso sistémico y meningioma petroclival izquierdo." Memorias del Instituto de Investigaciones en Ciencias de la Salud 19, no. 1 (2021): 74–78. http://dx.doi.org/10.18004/mem.iics/1812-9528/2021.019.01.74.

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El síndrome de Cotard es una entidad rara en la cual el paciente manifiesta ideas delirantes acerca de que se encuentra sin vida o que sus órganos internos se encuentran en estado de descomposición, entre otras alteraciones psicopatológicas. Existen diferentes reportes sobre el síndrome en diversas culturas y poblaciones. Usualmente tiene presentaciones neuropsiquiátricas y se lo identifica acompañando entidades neurológicas, metabólicas, infecciosas, entre otras. A través de este reporte de caso, se presenta una paciente con lupus eritematoso sistémico, que desarrolló este tipo de ideas delir

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25

Maia, J. "Cotard’s Syndrome - a Case Study." European Psychiatry 24, S1 (2009): 1. http://dx.doi.org/10.1016/s0924-9338(09)71175-7.

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Cotard"s Syndrome (CS) is a relatively rare but highly impressive psychopathological condition. It is characterized by the presence of nihilistic delusions concerning the body and the non-existence of the self, with general feelings of unreality and the belief that one is dead or the world no longer exists, hypochondrial delusions, ideas of guilt and immortality.First reported in 1880 by Jules Cotard, a French psychiatrist who described a "delire de negation", this clinical state was then believed to be a new type of agitated melancholia. Since then, similar cases have been reported worldwide

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26

Weiss, C., J. Santander, and R. Torres. "Catatonia, Neuroleptic Malignant Syndrome, and Cotard Syndrome in a 22-Year-Old Woman: A Case Report." Case Reports in Psychiatry 2013 (2013): 1–3. http://dx.doi.org/10.1155/2013/452646.

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The following case study describes a 22-year-old woman with depression and symptoms of psychosis who developed neuroleptic malignant syndrome after using Risperidone, thus requiring life support equipment and Bromocriptine, later recovering after seven days. From a psychiatric and neurological point of view, however, the persistence of catatonic syndrome and Cotard syndrome delusions was observed, based on assertions such as “I do not have a heart,” “my heart is not beating,” “I can not breathe,” “I am breaking apart,” “I have no head” (ideas of negation) and statements about the patient being

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Solla, Paolo, Antonino Cannas, Gianni Orofino, and Francesco Marrosu. "Fluctuating Cotard Syndrome in a Patient With Advanced Parkinson Disease." Neurologist 19, no. 3 (2015): 70–72. http://dx.doi.org/10.1097/nrl.0000000000000010.

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28

Ferro, Fillippo Maria. "Le corps en fragments dans le syndrome de Jules Cotard." L'Évolution Psychiatrique 68, no. 4 (2003): 579–89. http://dx.doi.org/10.1016/j.evopsy.2003.05.002.

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29

Chatterjee, Seshadri Sekhar, and Sayantanava Mitra. "“I Do Not Exist”—Cotard Syndrome in Insular Cortex Atrophy." Biological Psychiatry 77, no. 11 (2015): e52-e53. http://dx.doi.org/10.1016/j.biopsych.2014.11.005.

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30

Ferro, F. "Le corps en fragments dans le syndrome de Jules Cotard, Fragments of the body in Cotard's syndrom." L'Évolution Psychiatrique 68, no. 4 (2003): 579–89. http://dx.doi.org/10.1016/s0014-3855(03)00148-8.

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31

Pąchalska, Maria. "EVENT-RELATED POTENTIALS AS AN INDEX OF LOST COGNITIVE CONTROL AND LOST SELF IN A TBI PATIENT WITH DURATION INCREASING POST-TRAUMATIC DELUSIONAL MISIDENTIFICATION SYNDROME CONCLUDED WITH COTARD SYNDROME." Acta Neuropsychologica 17, no. 4 (2019): 487–508. http://dx.doi.org/10.5604/01.3001.0014.4268.

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The goal of the study was twofold: 1) to evaluate the QEEG/ ERPs indexes of functional brain impairment in a TBI patient diagnosed with chronic lost cognitive control and lost self caused by post traumatic, and here increasing over time, delusional misidentification syndrome concluded with Cotard syndrome in the blooming stage, with nihilistic delusions concerning the body and existence, and the delusion of being dead, and 2) to explore the mind of a patient whose identity has been disengaged, and who experiences the loss of his self and relations with his immediate surroundings with all the t

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32

Chandradasa, Miyuru, P. K. D. H. J. L. De Silva Rajaratne, Chirantha Kuruppuarachchi, and K. A. L. A. Kuruppuarachchi. "The living being dead: Cotard syndrome presenting as a dead spirit." Sri Lanka Journal of Medicine 29, no. 2 (2020): 83. http://dx.doi.org/10.4038/sljm.v29i2.197.

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33

MCGREAL, ANALISE E., MATTHEW K. BOLES, and IVETA BOYANCHEK. "Cotard Syndrome in an Adolescent With a First Episode of Psychosis." Journal of Psychiatric Practice 27, no. 3 (2021): 224–27. http://dx.doi.org/10.1097/pra.0000000000000545.

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34

Rodrigues, T., M. Passos, and H. Pereira. "Cotard’s Delusion: A Clinical and Conceptual Overview." European Psychiatry 24, S1 (2009): 1. http://dx.doi.org/10.1016/s0924-9338(09)70962-9.

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Background:In 1880, the French neurologist Jules Cotard described a specific kind of nihilistic delusion which the patient believed that she no longer existed. Since then, this rare condition known as Cotard's Syndrome or Cotard's Delusion (CD) has intrigued clinicians and investigators.Aims:To present CD's features, including historical, clinical, etiopathological, and treatment issues.Method:Case report of a 49-year-old woman with fully developed CD; review of the literature.Results:There is still a considerable debate concerning the nature of this phenomenon - whether it should be conceptua

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35

Billon, Alexandre. "Making Sense of the Cotard Syndrome: Insights from the Study of Depersonalisation." Mind & Language 31, no. 3 (2016): 356–91. http://dx.doi.org/10.1111/mila.12110.

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36

Fałkowska, Urszula, Katarzyna Adamczyk, Dorota Adamczyk, Ewelina Soroka, Véronique Petit, and Marcin Olajossy. "Uncommon psychopathological syndromes in psychiatry." Current Problems of Psychiatry 19, no. 4 (2018): 299–322. http://dx.doi.org/10.2478/cpp-2018-0024.

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Abstract Introduction: The development of biological sciences, as well as cultural and civilizational changes have led to the emergence of practice within the medicine of science, called psychiatry. Already at the turn of the 19th and the beginning of the 20th century, Karl Jaspers - a German scholar - father of psychopathology - in the work “Allgemeine Psychopathologie” crystallized his intuitions in the field of psychopathology, which classifies and describes states that are deviations from the physiological mental state of a human being. Material and method: his paper reviews available lite

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37

De Risio, S., M. Sarchiapone, G. Camardese, F. Calvosa, A. Buonanno, and E. Barbarino. "Successful pharmacotherapy of cotard syndrome with reduction of D2 receptors in basal ganglia." European Psychiatry 13, S4 (1998): 260s. http://dx.doi.org/10.1016/s0924-9338(99)80461-1.

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38

Perez, David L., Benjamin H. Fuchs, and Jane Epstein. "A Case of Cotard Syndrome in a Woman With a Right Subdural Hemorrhage." Journal of Neuropsychiatry and Clinical Neurosciences 26, no. 1 (2014): E29—E30. http://dx.doi.org/10.1176/appi.neuropsych.13020021.

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39

Gonçalves, Luís Moreira, and Alberto Tosoni. "Sudden onset of Cotard’s syndrome as a clinical sign of brain tumor." Archives of Clinical Psychiatry (São Paulo) 43, no. 2 (2016): 35–36. http://dx.doi.org/10.1590/0101-60830000000080.

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40

Risio, Sergio De, Giuseppe De Rossi, Marco Sarchiapone, et al. "A case of Cotard syndrome: 123I-IBZM SPECT imaging of striatal D2 receptor binding." Psychiatry Research: Neuroimaging 130, no. 1 (2004): 109–12. http://dx.doi.org/10.1016/j.pscychresns.2003.01.001.

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41

Pearn, J., and C. Gardner-Thorpe. "Jules Cotard (1840-1889): His life and the unique syndrome which bears his name." Neurology 58, no. 9 (2002): 1400–1403. http://dx.doi.org/10.1212/wnl.58.9.1400.

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42

Laios, Konstantinos, Gregory Tsoucalas, Dimitrios A. Vrachatis, Antonis Charalampakis, Gregory Androutsos, and Marianna Karamanou. "Are Drugs Always the Proper Solution to Therapeutic Dilemmas? Non-drug Approaches to the Post-traumatic Stress “Waking Corpse” Syndrome." Current Pharmaceutical Design 25, no. 1 (2019): 1–4. http://dx.doi.org/10.2174/138161282501190514091805.

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Jules Cotard (1840-1889), a Parisian neurologist, described a syndrome of delirium negations which was later named after him. Some physicians in antiquity and medieval times, especially in Asia, have noticed this syndrome and categorized it as a symptom of melancholy. They have presented it as a &quot;walking corpse syndrome&quot;, inflicting most probably veteran soldiers after suffering during ferocious battles, presenting the first cases of a post war traumatic stress disorder. Philotimus (3rd-2nd century BC) was the first to record it around 3rd century BC, and proposed a simple bu

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Dimitriadis, Yorgos. "The Painful Analgesia of Cotard’s Syndrome." Open Pain Journal 7, no. 1 (2014): 36–40. http://dx.doi.org/10.2174/1876386301407010036.

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In the present paper, we look into what is painful psychical analgesia in relation to what 19th century clinicians have named “moral pain” in melancholia, and more particularly in the delusion of negation described by the French psychiatrist Jules Cotard in 1880, a form of delusion that can be seen mostly in cases of chronic anxious melancholia. This condition is characterized by a painful absence of emotions, which occurs when the subject, in the Lacanian sense of the word, ceases to be touched by the signifiers, and consequently ceases to exist as a subject. Hence, these patients often decla

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Gardner-Thorpe, C., and J. Pearn. "The Cotard syndrome. Report of two patients: with a review of the extended spectrum of 'delire des negations'." European Journal of Neurology 11, no. 8 (2004): 563–66. http://dx.doi.org/10.1111/j.1468-1331.2004.00832.x.

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45

Hashioka, Sadayuki, Akira Monji, Masayuki Sasaki, Ichiro Yoshida, Kanji Baba, and Nobutada Tashiro. "A Patient With Cotard Syndrome Who Showed an Improvement in Single Photon Emission Computed Tomography Findings After Successful Treatment With Antidepressants." Clinical Neuropharmacology 25, no. 5 (2002): 276–79. http://dx.doi.org/10.1097/00002826-200209000-00011.

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46

Restrepo-Martínez, Miguel, Mariana Espinola-Nadurille, Leo Bayliss, et al. "FDG-PET in Cotard syndrome before and after treatment: can functional brain imaging support a two-factor hypothesis of nihilistic delusions?" Cognitive Neuropsychiatry 24, no. 6 (2019): 470–80. http://dx.doi.org/10.1080/13546805.2019.1676710.

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47

Trifu, Simona, Beligeanu Mihaela, Iacob Beatrice Ștefana, and Larimian Ștefania Parisa. "PARANOID SCHIZOPHRENIA -BETWEEN HYPERSEXUALITY AND SADOMASOCHISM." International Journal of Research -GRANTHAALAYAH 9, no. 3 (2021): 195–203. http://dx.doi.org/10.29121/granthaalayah.v9.i3.2021.3791.

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Motivation/Background: In this paper we aimed at clinically analyzing a patient diagnosed with paranoid schizophrenia, who also displays features specific to multiple personality disorders, in the context of a presentation whose key topic is sexuality. Given the global prevalence and the severity of schizophrenia, it is increasingly important to appropriately adapt and identify the patients' clinical and non-clinical personality profile. This paper also aims at making the profile of a patient diagnosed with axis I disorder ever since the age of 19, who also has got traits specific to certain p

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48

Kearns, Anthony. "Cotard's Syndrome in a Mentally Handicapped Man." British Journal of Psychiatry 150, no. 1 (1987): 112–14. http://dx.doi.org/10.1192/bjp.150.1.112.

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A mentally handicapped man with Cotard's syndrome is described, and the usefulness of electroconvulsive therapy in his management discussed. Even the more uncommon psychiatric syndromes such as this can be found in people with lower intellectual functioning, with clinical features little modified.

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Karakuła, Kaja Hanna, Małgorzata Romaniuk, Karol Krupa, Małgorzata Futyma-Jędrzejewska, and Dariusz Juchnowicz. "My Body Is Rotting: A case report of Cotard’s syndrome in a postpartum woman." Current Problems of Psychiatry 21, no. 2 (2020): 102–8. http://dx.doi.org/10.2478/cpp-2020-0010.

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AbstractIntroduction: Cotard’s syndrome (CS) is a rare set of psychopathological symptoms, the main symptom of which is nihilistic delusions concerning the negation of the existence of internal organs or the entire bodyAim, material and methodology: The aim of the study is to present a case of a patient treated for postpartum depression who developed Cotard’s syndrome. The patient’s symptoms began immediately after her daughter. The clinical picture was dominated by anxiety and apathy, nihilistic delusions about the atrophy of the urethra and other lower abdominal organs, and olfactory halluci

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Grover, Sandeep, Jitender Aneja, Sonali Mahajan, and Sannidhya Varma. "Cotard’s syndrome: Two case reports and a brief review of literature." Journal of Neurosciences in Rural Practice 05, S 01 (2014): S059—S062. http://dx.doi.org/10.4103/0976-3147.145206.

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ABSTRACTCotard’s syndrome is a rare neuropsychiatric condition in which the patient denies existence of one’s own body to the extent of delusions of immortality. One of the consequences of Cotard’s syndrome is self-starvation because of negation of existence of self. Although Cotard’s syndrome has been reported to be associated with various organic conditions and other forms of psychopathology, it is less often reported to be seen in patients with catatonia. In this report we present two cases of Cotard’s syndrome, both of whom had associated self-starvation and nutritional deficiencies and on

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