Moschopoulos N P, Kaprinis S, Nimatoudis J
3rd Department of Psychiatry, AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Psychiatriki. 2016 Oct-Dec;27(4):296-302. doi: 10.22365/jpsych.2016.274.296.
The term "Cotard's syndrome" is used to describe a number of clinical features, mostly hypochondriac and nihilistic delusions, the most characteristic of which are the ideas "I am dead" and "my internal organs do not exist". Besides, anxious and depressed mood, delusions of damnation, possession and immortality, suicidal and self-mutilating behavior are included. The first description of the syndrome was made in 1880 by Cotard, who presented the case of a female patient in a lecture. He originally named it "hypochondriac delusion", and some years later "delusion of negations", while it was named "Cotard delusion" after his death. In international literature, the terms "nihilistic delusion" and "Cotard's syndrome" prevailed over "delusion of negations" and "Cotard delusion". In the present study we report the case of a 59 year-old woman, who was admitted to our department after a suicide attempt, and who showed symptoms of Cotard's syndrome for about two years, namely depressed mood, hypochondriac and nihilistic delusions, delusions of immortality and damnation, suicidal ideation, severe psychomotor retardation, diminished motivation and tendency to stay in bed. She never took the medication she was prescribed, and at times she refused to eat. During her hospitalization, there was performed a full blood panel and medical imaging, that showed chronic ischemic infarctions, periventricular leukoencephalopathy and diffuse cerebral atrophy in MRI. All the other test results were normal. She was administered treatment with haloperidol, mirtazapine and venlafaxine. Gradually, her psychomotor ability, motivation and mood improved, she didn't express suicidal ideation, her delusions were less intense and she was able to question them, but they weren't eliminated. She was discharged in improved condition, after 44 days. Cotard's syndrome isn't mentioned in the current classification systems (ICD-10, DSM-5). In literature though, it has been divided into three types, according to the clinical symptoms: psychotic depression, Cotard type I, and Cotard type II, and three stages have been proposed: germination stage, blooming stage and chronic stage. It has been associated with various medical conditions, such as cerebral infractions, frontotemporal atrophy, epilepsy, encephalitis, brain tumors, traumatic brain injury. Furthermore, it has been associated with psychiatric conditions, such as mental retardation, postpartum depression, depersonalization disorder, catatonia, Capgras syndrome, Fregoli syndrome, Odysseus syndrome, koro syndrome. Several reports about successful pharmacological treatments have been published, both monotherapies with antidepressants, antipsychotics or lithium, and by antidepressant and antipsychotic combination treatments. The most reported successful treatment strategy for Cotard's syndrome is electroconvulsive therapy (ECT), administration of which should follow current treatment guidelines of the underlying conditions.
“科塔尔综合征”一词用于描述多种临床特征,主要是疑病和虚无妄想,其中最具特征性的是“我死了”和“我的内脏不存在”的想法。此外,还包括焦虑和抑郁情绪、诅咒妄想、附身妄想和不朽妄想、自杀和自残行为。该综合征最早由科塔尔于1880年描述,他在一次讲座中介绍了一名女性患者的病例。他最初将其命名为“疑病妄想”,几年后又称为“否定妄想”,而在他去世后被命名为“科塔尔妄想”。在国际文献中,“虚无妄想”和“科塔尔综合征”这两个术语比“否定妄想”和“科塔尔妄想”更为常用。在本研究中,我们报告了一名59岁女性的病例,她在自杀未遂后入住我们科室,出现科塔尔综合征症状约两年,即情绪低落、疑病和虚无妄想、不朽和诅咒妄想、自杀观念、严重的精神运动迟缓、动机减退和卧床倾向。她从未服用过开给她的药物,有时还拒绝进食。在她住院期间,进行了全血细胞检查和医学影像检查,MRI显示有慢性缺血性梗死、脑室周围白质脑病和弥漫性脑萎缩。所有其他检查结果均正常。她接受了氟哌啶醇、米氮平和文拉法辛的治疗。逐渐地,她的精神运动能力、动机和情绪有所改善,不再表达自杀观念,妄想强度减轻,能够对其提出质疑,但并未消除。44天后,她病情好转出院。当前的分类系统(ICD - 10、DSM - 5)中未提及科塔尔综合征。不过在文献中,根据临床症状它被分为三种类型:精神病性抑郁、科塔尔I型和科塔尔II型,并且提出了三个阶段:萌芽期、盛开期和慢性期。它与多种医学状况相关,如脑梗死、额颞叶萎缩、癫痫、脑炎、脑肿瘤、创伤性脑损伤。此外,它还与一些精神疾病相关,如智力发育迟缓、产后抑郁、人格解体障碍、紧张症、卡普格拉综合征、弗雷戈里综合征、奥德修斯综合征以及缩阳症。已经发表了多篇关于成功药物治疗的报告,包括使用抗抑郁药、抗精神病药或锂盐的单一疗法,以及抗抑郁药和抗精神病药的联合治疗。报道最多的科塔尔综合征成功治疗策略是电休克治疗(ECT),其应用应遵循潜在疾病当前的治疗指南。