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Addictive (Non-Drug) and Obsessive-Compulsive Symptoms after Focal Brain Lesions. 局灶性脑损伤后的成瘾(非药物)和强迫症状。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2017-11-16 DOI: 10.1159/000475697
René M Müri, Dario Cazzoli

This chapter presents an overview of different addictive and obsessive-compulsive symptoms and their constellations due to focal brain lesions. In general, such symptoms are not systematically reported in the literature, and the knowledge about the networks involved is sometimes sparse. Finally, we present an original case with an unusual combination of kleptomania and hyper-religiosity.

本章概述了由局灶性脑损伤引起的不同的成瘾和强迫症状及其星座。一般来说,这些症状在文献中没有系统的报道,并且对所涉及的网络的知识有时是稀疏的。最后,我们提出一个原始的情况下,一个不寻常的组合盗窃狂和超宗教。
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引用次数: 0
Violent Behavior. 暴力行为。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2017-11-17 DOI: 10.1159/000475696
Sophia Sopromadze, Alexander Tsiskaridze

Violence is a significant public health problem representing one of the leading causes of death worldwide for people aged 15-44 years. Although violence and aggression are more frequent in adolescence and early adult life and decline with advancing age, these conditions can still develop for the first time in old age especially in association with organic brain disorder. Rates of violent death vary according to country income levels and are twice as higher in low- to middle-income countries than in high-income countries. Males are more affected than females. Violence is a multifactorial condition. A combination of biologic, psychodynamic, and social factors may play a role in development of violence and aggression. Since it may accompany or be result of different medical conditions it is important to determine the underlying condition or disease including mental illness for targeting the proper therapeutic strategy. In the acute setting with a behavioral emergency the primary task for the clinician is to act as soon as possible in order to stop the violence from escalating and to find the quickest way to keep the patient's agitation and violence under control with the maximum of safety for everybody using the less severe yet effective interventions. Multiple steps of talk down interventions and non-coercive behavioral and environmental treatments have been proposed. If such an approach is not effective, more coercive interventions are needed including involuntary medications and chemical restrain as well as physical restraint or seclusion in some cases.

暴力是一个重大的公共卫生问题,是全世界15-44岁人群死亡的主要原因之一。尽管暴力和攻击行为在青春期和成年早期更为频繁,并随着年龄的增长而减少,但这些情况仍可能在老年时首次出现,特别是与器质性脑障碍有关。暴力死亡率因国家收入水平而异,中低收入国家的暴力死亡率是高收入国家的两倍。男性比女性更容易受到影响。暴力是一种多因素的情况。生物、心理动力学和社会因素的结合可能在暴力和攻击的发展中起作用。由于它可能伴随或由不同的医疗条件的结果,重要的是确定潜在的条件或疾病,包括精神疾病,以针对适当的治疗策略。在行为紧急的急性环境中,临床医生的主要任务是尽快采取行动,以阻止暴力升级,并找到最快的方法,以最大限度地安全控制患者的躁动和暴力,使用不那么严重但有效的干预措施。提出了多步骤的谈话干预和非强制性行为和环境治疗。如果这种方法无效,则需要采取更多的强制性干预措施,包括非自愿用药和化学限制,以及在某些情况下进行身体限制或隔离。
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引用次数: 4
Possessions Including Poltergeist: "Are You There, Madness?" 包括鬼语:“你在吗,疯狂?”
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2017-11-17 DOI: 10.1159/000475687
Olivier Walusinski

Beliefs involving the devil and possession figured in the nosography of mental illness that alienists gradually established during the 19th century. The description of this form of cenesthetic hallucination resulted in "the possessed" being viewed as patients, which protected them from the trials and punishments they so frequently faced in earlier centuries. According to psychologists, this illusion of mental duality is linked to impairment of introspective capacities. Current brain imaging suggests inappropriate activity of the default mode network, which interferes with attentional systems during the hallucinatory episode.

涉及魔鬼和附身的信仰出现在19世纪异己主义者逐渐建立起来的精神疾病的分类学中。对这种形式的感官幻觉的描述导致“被附身者”被视为病人,这使他们免受他们在早期经常面临的审判和惩罚。根据心理学家的说法,这种精神二元性的错觉与内省能力的损害有关。目前的脑成像显示,默认模式网络的不适当活动,在幻觉发作期间干扰了注意系统。
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引用次数: 0
REM Sleep Behavior Disorder. 快速眼动睡眠行为障碍。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2017-11-16 DOI: 10.1159/000478914
Claudio L Bassetti, Panagiotis Bargiotas

Rapid eye movement sleep behavior disorder (RBD) is a brain disorder, characterized by the dream enactment during rapid eye movement (REM) sleep due to a lack of physiologic muscle atonia and increased muscle twitching. Schenk was the first to describe this disorder in 1986; however, few authors reported in the 1970-1980s loss of physiological muscle atonia combined with dream enactment in the course of brainstem disorders and as a consequence of alcoholism and antidepressant treatment. RBD affects less than 1% of the adult population, but can be found in up to 25-50% of neurodegenerative disorders including Parkinson's disease, multisystem atrophy, and dementia with Lewy body. In the last decade, many studies provided evidence that RBD precedes parkinsonian motor signs by several years, suggesting that RBD should no longer be considered a complication but a part of the prodromal phase of these diseases. Etiologically, primary (idiopathic RBD) and several secondary forms in addition to neurodegeneration (related to focal brainstem damage, narcolepsy, autoimmune disorders, and drugs) are known. Pathophysiologically, brainstem and supratentorial mechanisms involving glutamatergic, glycinergic, and GABA-ergic neurotransmission have been implicated. Recently, an animal model of RBD has been described. Clinical features consist of characteristic nocturnal behaviors, but also daytime symptoms including excessive sleepiness and cognitive alterations. The diagnosis of RBD is made according to international diagnostic criteria, based on medical history, and video-polysomnographic features. Current treatment strategies include actions which ensure a safe sleep environment, the avoidance of triggering/exacerbating factors and if necessary pharmacological (mainly clonazepam and melatonin) and non-pharmacological (e.g., behavioral measures) interventions. Future research should clarify the exact sleep-wake characteristics of RBD (also beyond REM sleep) and their evolution over time, the contribution of brainstem but also supratentorial mechanisms to its pathophysiology, and the (early?) diagnostic and (causative?) treatment consequences of RBD in the context of neurodegeneration.

快速眼动睡眠行为障碍(Rapid eye movement sleep behavior disorder, RBD)是一种脑部疾病,其特征是在快速眼动(REM)睡眠期间由于缺乏生理性肌肉张力和肌肉抽搐增加而导致做梦。申克是1986年第一个描述这种疾病的人;然而,在1970- 80年代,很少有作者报道在脑干疾病过程中,酒精中毒和抗抑郁药物治疗导致生理性肌肉张力丧失并伴有做梦。RBD影响不到1%的成年人口,但可在高达25-50%的神经退行性疾病中发现,包括帕金森病、多系统萎缩和路易体痴呆。在过去的十年中,许多研究提供的证据表明,RBD早于帕金森运动体征数年,这表明RBD不应再被视为并发症,而应被视为这些疾病前驱期的一部分。病因学上,除了神经退行性疾病(与局灶性脑干损伤、发作性睡病、自身免疫性疾病和药物有关)外,原发性(特发性RBD)和几种继发性RBD是已知的。病理生理学上,脑干和幕上机制涉及谷氨酸能、甘氨酸能和氨基丁酸能神经传递。最近,一种RBD动物模型被描述。临床特征包括典型的夜间行为,但也有白天症状,包括过度嗜睡和认知改变。RBD的诊断是根据国际诊断标准,基于病史和视频多导睡眠图特征。目前的治疗策略包括确保安全睡眠环境的行动、避免触发/加重因素以及必要时的药理学(主要是氯硝西泮和褪黑激素)和非药理学(例如行为措施)干预措施。未来的研究应该明确RBD的确切睡眠-觉醒特征(也包括快速眼动睡眠之外的睡眠)及其随时间的演变,脑干和幕上机制对其病理生理的贡献,以及在神经变性背景下RBD的(早期)诊断和(病因)治疗后果。
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引用次数: 18
Raymond Roussel's Cure with Pierre Janet. Raymond Roussel的Cure和Pierre Janet。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2018-10-18 DOI: 10.1159/000490442
Jean-Pierre Luauté

Raymond Roussel (1877-1933) was an eccentric writer whose strange novelistic and theatrical work was launched by the surrealists and is still worshipped by the French intelligentia. While writing his first text at the age of 19 years, he presented a delusional episode marked by the conviction that he was shining like a sun and that he had acquired universal glory. He "fell back to earth" when the book was published and he realized that no one was stopping to gaze at him. He later led a ritualized life, continuing to write and eventually achieving success - glory even - with the champions of the surrealist revolution, who saw the genius in him. His eccentricities, permitted by his immense fortune, contributed to the legend and helped him to exist socially. He was also able to conceal his homosexuality, which appears to be closely dependent on an emotional infantilism. His pathology is recognized thanks to Pierre Janet's account (1859-1947) of his case in De l'Angoisse à l'Extase. Janet's accompanying psychotherapy, which supported him for many years, was effective in moving him towards a form of obsessive consolidation. Janet's therapeutic approach, however, is currently strongly criticized by dogmatic psychoanalysts. Roussel must have been aware of the artificial nature of his theatrical successes and he succumbed to a depressive state, taking refuge in barbiturate addiction. He died in a Palermo hotel room of a barbiturate overdose, considered to be suicidal.

雷蒙德·鲁塞尔(1877-1933)是一位古怪的作家,他的怪诞小说和戏剧作品是由超现实主义者发起的,至今仍受到法国知识界的崇拜。在他19岁写第一篇文章的时候,他出现了一种错觉,认为自己像太阳一样闪闪发光,获得了普遍的荣耀。当这本书出版时,他“回到了现实”,他意识到没有人停下来盯着他看。他后来过着一种仪式化的生活,继续写作,并最终与超现实主义革命的捍卫者一起取得了成功,甚至是荣耀,他们看到了他的天才。他的怪癖,在他巨大的财富允许下,促成了这个传说,并帮助他在社会上生存。他还能够隐藏自己的同性恋,这似乎与情感上的幼稚症密切相关。由于皮埃尔·珍妮特(Pierre Janet)在《De l'Angoisse / l'Extase》中对他的病例的描述(1859-1947),他的病理得到了认可。珍妮特伴随的心理治疗支持了他多年,有效地将他推向了一种强迫性巩固的形式。然而,珍妮特的治疗方法目前受到教条主义精神分析学家的强烈批评。鲁塞尔一定意识到他在戏剧上的成功是人为的,他陷入了抑郁状态,以巴比妥酸盐成瘾来寻求庇护。他死于巴勒莫一家酒店的房间,死因是巴比妥酸盐过量,被认为是自杀。
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引用次数: 0
Machado de Assis' Original Sin. 马查多·德·阿西斯的原创作品。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2018-10-18 DOI: 10.1159/000490685
Gabriel R de Freitas

Machado de Assis (1839-1908) suffered from temporal lobe epilepsy, probably with origin in the non-dominant hemisphere. The evidence for this is provided by the detailed reports of the characteristics of his seizures by his contemporaries and by his correspondence with other writers. He was treated with bromides and homeopathy. It is unclear whether his neurological disorder influenced his artistic performance. What is evident is that he was deeply ashamed of the disease - he avoided the word "epilepsy" and just wrote about it in his personal correspondence with friends in the last years of his life. Though controversial, he had no clear traces of personality disorders linked to his temporal lobe epilepsy. Despite all his adversities, including being "mulatto," having a stutter, being of humble origins, and epileptic in a period when there was no efficacious therapy and a profound stigma associated with the disease, Machado de Assis became one of the most important Brazilian writers of all times.

Machado de Assis(1839-1908)患有颞叶癫痫,可能起源于非优势半球。他的同时代人对他癫痫发作特征的详细报告以及他与其他作家的通信都提供了证据。他用溴化物和顺势疗法治疗他。目前尚不清楚他的神经紊乱是否影响了他的艺术表现。显而易见的是,他对这种疾病深感羞愧——他避免使用“癫痫”这个词,只是在他生命的最后几年里,在与朋友的私人通信中提到了它。尽管存在争议,但他没有明显的与颞叶癫痫有关的人格障碍迹象。马查多·德·阿西斯尽管遭遇了种种逆境,包括他是“混血”,口吃,出身卑微,在没有有效治疗方法的时期患有癫痫,以及与这种疾病相关的深刻耻辱,但他成为了巴西有史以来最重要的作家之一。
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引用次数: 0
Dissociation, Delusion and the Splitting of the Self in The Trial by Franz Kafka: Phenomenology and Neurobiology of Schizophrenia. 卡夫卡《审判》中的分离、妄想与自我分裂:精神分裂症的现象学与神经生物学。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2018-10-18 DOI: 10.1159/000490450
Elisabete Castelon Konkiewitz, Edward Benjamin Ziff

In this essay, we propose an association between Franz Kafka's novel, The Trial, and phenomenological and neurobiological processes in schizophrenia. We begin by presenting a summary of the plot, pointing to some of its remarkable literary aspects. We next compare the mental processes of dissociation, disorientation and delusion as represented in the novel with phenomenological processes that take place in the prodromal states of schizophrenia. We discuss how such disorders of the self and disorders of thought, both crucial aspects of the schizophrenic experience, appear in The Trial and in other literary and private writings by Franz Kafka. We relate how these disorders may arise from the false attribution of salience and false associative learning caused by hyperactivity of dopaminergic function associated with chaotic firing of dopaminergic neurons. Finally, we show how Kafka leads not just the protagonist of The Trial, but even more the reader to experience a quasi-delusional state. We discuss the relationship between the perturbation of thought and disorientation of mind evoked by the novel in the reader and the need of our brains for empathy and predictability.

在本文中,我们提出了卡夫卡的小说《审判》与精神分裂症的现象学和神经生物学过程之间的联系。我们首先对故事情节做一个总结,指出其中一些引人注目的文学方面。接下来,我们将小说中所呈现的精神分离、迷失方向和妄想的心理过程与精神分裂症前驱状态的现象学过程进行比较。我们将讨论精神分裂症经历的两个重要方面——自我的混乱和思想的混乱——是如何出现在《审判》以及卡夫卡的其他文学和私人作品中。我们将这些障碍与多巴胺能神经元的混乱放电相关的多巴胺能功能亢进引起的显著性错误归因和虚假联想学习联系起来。最后,我们展示了卡夫卡如何不仅引导《审判》的主人公,而且更多地引导读者体验一种准妄想状态。我们讨论了小说在读者中引起的思想扰动和精神迷失与我们大脑对移情和可预测性的需求之间的关系。
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引用次数: 1
Travelling into Alienation and Neurology with a Painter: Georges Moreau (1848-1901). 与画家一起进入异化和神经学:乔治·莫罗(1848-1901)。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2018-10-18 DOI: 10.1159/000490439
Olivier Walusinski

Georges Moreau (1848-1901) was a painter and the son of the famous psychiatrist Jacques-Joseph Moreau de Tours. Early in his career, his paintings aspired toward figurative perfection, exalting patriotic and historical themes. His prolific production includes numerous paintings for which he drew inspiration from psychology and certain mental pathologies. At the age of 45 years he suffered right hemiplegia which forced him to set aside large-scale subjects and focus instead on intimist, almost pointillistic works, which brought him closer to the Impressionists, as his portrait of Paul Cézanne shows. Possibly his most well-known painting, Les fascinés de la Charité, service du Dr. Luys, is analysed here by comparison with La Leçon clinique à La Salpêtrière by André Brouillet, which depicts Jean-Martin Charcot and his students.

乔治·莫罗(1848-1901)是一位画家,也是著名精神病学家雅克-约瑟夫·莫罗·德图尔的儿子。在他职业生涯的早期,他的绘画追求形象的完美,颂扬爱国主义和历史主题。他多产的作品包括许多绘画,他从心理学和某些精神病理学中汲取灵感。45岁时,他患上了右半瘫,这迫使他放弃了大规模的主题,转而专注于内线主义,几乎是点画主义的作品,这使他更接近印象派,就像他画的保罗·卡萨恩的肖像所显示的那样。可能是他最著名的画作,Les fascin de la charit, service du Dr. Luys,在这里通过与andr Brouillet的la leon clinique la Salpêtrière进行比较来分析,这幅画描绘了让-马丁·沙科和他的学生。
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引用次数: 2
Henrik Ibsen's Battle with Cerebrovascular Disease. 易卜生与脑血管疾病的斗争。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2018-10-18 DOI: 10.1159/000490444
Jan C Frich

Henrik Ibsen (1828-1906) is a Norwegian playwright and poet who is known as the father of modern drama. Ibsen was in good health when he announced at his 70th birthday celebration that he intended to continue writing. His last play, When We Dead Awaken, was published in 1899. Why did Ibsen's dramatic writing come to an end? This chapter presents a medical account of Ibsen's health condition during the last 6 years of his life. It is based on a review of a document written by one of his doctors, Edvard Bull (1845-1925), letters, biographic information, and Ibsen's death certificate. The historical material suggests that he suffered from arteriosclerosis and cerebrovascular disease, and that he suffered several strokes, in 1900, 1901, and 1903. He suffered a paresis in his left foot, expressive aphasia, and a right hemiparesis, and he lost the ability to write. There is no evidence that Ibsen was hospitalised. He received medical treatment and care at his home and at a recreational spa. His health condition was unstable, and it is likely that he suffered from a series of smaller strokes in the last years of his life. Ibsen developed signs of heart failure, and he died peacefully from "paralysis cordis" at his home on May 23rd, 1906.

易卜生(1828-1906)是挪威剧作家和诗人,被誉为现代戏剧之父。易卜生在70岁生日庆典上宣布他打算继续写作时,身体状况良好。他的最后一部戏剧《当我们死去醒来》出版于1899年。易卜生的戏剧创作为何走向终结?本章介绍了易卜生在生命最后6年里的健康状况。这本书是根据易卜生的一位医生爱德华·布尔(edward Bull, 1845-1925)写的一份文件、信件、传记信息和易卜生的死亡证明编写的。历史资料表明,他患有动脉硬化和脑血管疾病,并在1900年、1901年和1903年多次中风。他患有左脚麻痹、表达性失语症和右半瘫,他失去了写作的能力。没有证据表明易卜生曾住院。他在家中和一家休闲水疗中心接受了治疗和护理。他的健康状况不稳定,很可能在他生命的最后几年遭受了一系列较小的中风。易卜生出现了心脏衰竭的迹象,他于1906年5月23日在家中平静地死于“麻痹性心衰”。
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引用次数: 0
Cotard Syndrome. 科塔尔综合症。
Q3 Medicine Pub Date : 2018-01-01 Epub Date: 2017-11-17 DOI: 10.1159/000475679
Sebastian Dieguez

Cotard's syndrome is often described as the delusional belief that one is dead or non-existent. However, Jules Cotard's initial description (1880) of the "delusion of negations" was much richer and also involved delusions and claims of immortality and enormity, feelings of damnation, and illusions of bodily dissolution and transformation. Alternatively conceived as an extreme case of depression, hypochondria, or psychosis, the condition is considered rare and remains poorly understood. Cotard himself provided a taxonomy and several explanations for the condition, focusing on its distinction from classical persecutory delusions and suggesting that it could be a kind of reversed grandiosity. He proposed a psychosensory basis in the dissolution of mental imagery, which he then extended to a more general psychomotor impairment of volition. Other early authors highlighted a disorder of the bodily self, and more recent theories postulated an impairment of right hemispheric functions, leading to perceptual and somatosensory feelings of unreality, which coupled with reasoning impairments and an internalized attributional style led in turn to beliefs of non-existence. However, despite its striking presentation and its relevance to our understanding of self-awareness, Cotard's syndrome remains an elusive condition, rarely reported and poorly researched.

科塔尔综合症通常被描述为一种妄想,认为自己已经死亡或不存在。然而,儒勒·科塔尔(Jules Cotard)对“否定妄想”的最初描述(1880年)要丰富得多,还包括对不朽和巨大的妄想和主张,诅咒的感觉,以及身体解体和转变的幻觉。作为一种抑郁症、疑病症或精神病的极端情况,这种情况被认为是罕见的,并且仍然知之甚少。科塔尔自己也为这种情况提供了分类和几种解释,重点是它与经典的迫害妄想的区别,并暗示它可能是一种反向的夸大。他提出了心理意象分解的心理感觉基础,然后将其扩展到更普遍的意志精神运动障碍。其他早期的作者强调了身体自我的紊乱,而最近的理论则假设了右半球功能的损伤,导致了对不真实的感知和身体感觉,再加上推理障碍和内化归因风格,导致了不存在的信念。然而,尽管其引人注目的表现及其与我们对自我意识的理解相关,科塔尔综合征仍然是一种难以捉摸的疾病,很少报道和研究。
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引用次数: 17
期刊
Frontiers of Neurology and Neuroscience
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