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病例报告:双相情感障碍作为伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)的首发表现。

Case report: bipolar disorder as the first manifestation of CADASIL.

作者信息

Park Soyeon, Park Boram, Koh Min Kyung, Joo Yeon Ho

机构信息

Department of Psychiatry, University of Ulsan College of Medicine, Asan Medical Center, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 136-736, Korea.

出版信息

BMC Psychiatry. 2014 Jun 14;14:175. doi: 10.1186/1471-244X-14-175.

Abstract

BACKGROUND

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited cerebrovascular disease, clinically characterized by variable manifestations of migraine, recurrent transient ischemic attack or lacunar strokes, cognitive decline, and mood disturbances. However, manic episodes have rarely been documented as an initial symptom of CADASIL and bipolar disorder presenting as the first manifestation in CADASIL has not been reported previously from evaluations by psychiatrists or psychological testing by psychologists.

CASE PRESENTATION

A 53 year old woman developed symptoms of mania in her 50s leading to a personality change involving a continuously labile mood and irritability over a number of years. Neuropsychological testing revealed an intact memory, but impairment in attention and executive function. In the Rorschach test, she showed a high level of cognitive rigidity. Magnetic resonance imaging findings were very consistent with a diagnosis of CADASIL, which was confirmed by genetic testing for NOTCH3 mutations. Atypical antipsychotics proved to be helpful in treating her manic symptoms and for behavior control.

CONCLUSION

We present a novel case of CADASIL that first presented as bipolar disorder. We contend that when patients show a late onset personality change or chronically irritable mood that deteriorates over many years, an organic cause such as CADASIL must be considered. Further studies are needed to better understand the exact impacts of cerebral tissue lesions and psychiatric symptoms in CADASIL patients.

摘要

背景

大脑常染色体显性动脉病伴皮质下梗死和白质脑病(CADASIL)是一种遗传性脑血管疾病,临床特征为偏头痛、复发性短暂性脑缺血发作或腔隙性卒中、认知功能下降和情绪障碍等多种表现。然而,躁狂发作很少被记录为CADASIL的初始症状,且CADASIL中以双相情感障碍为首发表现此前尚未有精神科医生评估或心理学家心理测试的相关报道。

病例报告

一名53岁女性在50多岁时出现躁狂症状,导致性格改变,多年来情绪持续不稳定且易怒。神经心理学测试显示其记忆力完好,但注意力和执行功能受损。在罗夏测试中,她表现出高度的认知僵化。磁共振成像结果与CADASIL的诊断非常一致,通过NOTCH3基因突变的基因检测得以证实。非典型抗精神病药物被证明有助于治疗她的躁狂症状和控制行为。

结论

我们报告了一例首例表现为双相情感障碍的CADASIL新病例。我们认为,当患者出现晚年人格改变或多年来逐渐恶化的慢性易怒情绪时,必须考虑像CADASIL这样的器质性病因。需要进一步研究以更好地了解CADASIL患者脑组织病变和精神症状的确切影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1440/4080756/2cbb40fc6885/1471-244X-14-175-1.jpg

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