Stress cardiomyopathy (takotsubo cardiomyopathy).

Samer Khouri, Naser Imran
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引用次数: 6

Abstract

Background: Due to the rise in the number of reports of stress cardiomyopathy in the literature, awareness of this condition is increasing. Although different names have been used to describe this condition, the similarities in clinical, electrocardiographic, echocardiographic, and angiographic features suggest that they represent the same spectrum of diseases with different underlying causes. The pathophysiology of stress cardiomyopathy remains controversial.

Methods: We describe a series of four cases of stress cardiomyopathy admitted to our institution over a period of six months with different presentations, but similar clinical course, EKG, echocardiographic, and catheterization findings. The ages ranged from 22 to 81 years; all four females. All showed characteristic wall motion abnormalities by imaging in the absence of significant coronary artery disease, with spontaneous recovery of left ventricular function with conservative therapy.

Results: Although the patients presented with different clinical scenarios, all four showed characteristic features of stress cardiomyopathy suggesting that the pathophysiology affecting the myocardium was the same. We present a review of the literature with a discussion of the history of this condition, characteristic clinical features, and diagnostic criteria used in the past as well as the suggested pathophysiology of this condition.

Conclusion: Stress cardiomyopathy is an underdiagnosed reversible cardiomyopathy triggered by severe emotional or physical stress. It represents a spectrum of conditions with reversible severe left ventricular systolic dysfunction that includes neurogenic cardiomyopathy. It is not confined to the Japanese population and can affect people of any ethnic background or nationality.

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应激性心肌病(takotsubo心肌病)。
背景:由于文献中关于应激性心肌病的报道越来越多,人们对这种疾病的认识也越来越高。虽然不同的名称被用来描述这种情况,但在临床、心电图、超声心动图和血管造影特征上的相似性表明,它们代表了不同潜在原因的同一谱系疾病。应激性心肌病的病理生理学仍有争议。方法:我们报告了在6个月的时间里收治的4例应激性心肌病患者,他们的表现不同,但临床过程、心电图、超声心动图和导管检查结果相似。年龄从22岁到81岁不等;四只都是雌性。在没有明显冠状动脉疾病的情况下,所有患者均表现出特征性的壁运动异常,经保守治疗后左心室功能自行恢复。结果:虽然4例患者临床表现不同,但均表现出应激性心肌病的特征,提示影响心肌的病理生理是相同的。我们对文献进行了回顾,讨论了这种疾病的历史、典型的临床特征、过去使用的诊断标准以及这种疾病的病理生理学。结论:应激性心肌病是一种由严重的情绪或身体压力引起的未被诊断的可逆性心肌病。它代表了一系列可逆的严重左心室收缩功能障碍,包括神经源性心肌病。它并不局限于日本人口,可以影响任何种族背景或国籍的人。
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