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克莱恩-莱文综合征与双相障碍:反复发作和抵抗性抑郁的鉴别诊断。

Kleine-Levin syndrome and bipolar disorder: a differential diagnosis of recurrent and resistant depression.

机构信息

INSERM, U955, Créteil, France; AP-HP, Hôpital H. Mondor - A. Chenevier, Pôle de Psychiatrie, Créteil, France; Pôle de Psychiatrie, Univ Lille Nord de France, CHRU de Lille, Lille, France; Fondation FondaMental, Créteil, France.

出版信息

Bipolar Disord. 2013 Dec;15(8):899-902. doi: 10.1111/bdi.12119. Epub 2013 Sep 6.

Abstract

OBJECTIVES

Kleine-Levin syndrome (KLS) is a rare sleep disorder (1-2 reported cases per one million individuals) primarily affecting young subjects. Episodes are characterized by hypersomnia, cognitive impairment, feelings of derealization, and, less frequently, hyperphagia (66%), hypersexuality [53% (principally men)], and depressed mood [53% (predominantly women)]. KLS cases are frequently misdiagnosed and pose therapeutic challenges (i.e., amantadine and mood stabilizers are only marginally effective). The cause of KLS is unknown, but an association between KLS and mood disorders has been suggested by some clinical analogies.

METHODS

We report the case of a 44-year-old Caucasian woman with bipolar I disorder referred by her psychiatrist to our psychiatric center for recurrent and resistant major depression according to DSM-IV-TR criteria.

RESULTS

Following examination, we confirmed the diagnoses of bipolar I disorder and KLS. The patient experienced about 15 evenly distributed KLS episodes, each lasting about one week, which occurred during the six years following her first manifestation at age 18 years. An electroencephalogram was performed during a KLS episode and showed high-amplitude theta waves in the left and right temporal lobes, with predominance in the left hemisphere. The pronounced bipolar disorder symptomatology, starting at 15 years of age with major depression and a suicide attempt, had impeded the identification of KLS, which was not diagnosed until the age of 42.

CONCLUSIONS

Bipolar disorder may obscure KLS, with each condition adversely affecting the course of the other, and consequently, the co-occurrence of KLS and bipolar disorder may be underestimated. KLS and bipolar disorder may share common vulnerability factors, such as immune-inflammatory and circadian disturbances, and there may be a genetic predisposition for both. Additionally, mood stabilizers may be effective for KLS and bipolar disorder.

摘要

目的

克莱恩-莱文综合征(KLS)是一种罕见的睡眠障碍(每百万个体中报告 1-2 例),主要影响年轻患者。发作的特征是嗜睡、认知障碍、现实感丧失,以及较少见的食欲亢进(66%)、性欲亢进[53%(主要是男性)]和情绪低落[53%(主要是女性)]。KLS 病例经常被误诊,并且治疗具有挑战性(即金刚烷胺和心境稳定剂仅略有疗效)。KLS 的病因尚不清楚,但一些临床类比表明 KLS 与心境障碍之间存在关联。

方法

我们报告了一例 44 岁的白种女性,患有 I 型双相情感障碍,根据 DSM-IV-TR 标准,她的精神科医生将她转诊到我们的精神科中心,以治疗反复发作和耐药的重度抑郁症。

结果

经过检查,我们确认了双相 I 型障碍和 KLS 的诊断。该患者经历了约 15 次均匀分布的 KLS 发作,每次发作持续约一周,发生在她 18 岁首次发病后的六年中。在 KLS 发作期间进行了脑电图检查,显示左、右颞叶有高振幅θ波,左半球为主。明显的双相情感障碍症状,从 15 岁开始表现为重度抑郁症和自杀未遂,阻碍了 KLS 的诊断,直到 42 岁才确诊。

结论

双相情感障碍可能会掩盖 KLS,每种疾病都会对另一种疾病的病程产生不利影响,因此,KLS 和双相情感障碍的共同发生可能被低估了。KLS 和双相情感障碍可能具有共同的易感性因素,例如免疫炎症和昼夜节律紊乱,并且两者可能都有遗传倾向。此外,心境稳定剂可能对 KLS 和双相情感障碍有效。

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