Khouri Samer, Imran Naser
Division of Cardiovascular Medicine, University of Toledo, Toledo, Ohio, USA.
Clin Med Cardiol. 2009 Sep 17;3:93-9. doi: 10.4137/cmc.s3324.
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.
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.
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.
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.
由于文献中应激性心肌病报告数量的增加,对这种疾病的认识正在提高。尽管曾使用不同的名称来描述这种疾病,但临床、心电图、超声心动图和血管造影特征的相似性表明,它们代表了具有不同潜在病因的同一类疾病谱。应激性心肌病的病理生理学仍存在争议。
我们描述了一系列4例应激性心肌病患者,在6个月的时间里入住我们的机构,他们表现各异,但临床病程、心电图、超声心动图和导管检查结果相似。年龄范围为22至81岁;均为女性。所有患者在无明显冠状动脉疾病的情况下,通过影像学检查均显示出特征性的室壁运动异常,经保守治疗后左心室功能可自发恢复。
尽管患者表现出不同的临床情况,但所有4例均显示出应激性心肌病的特征性表现,提示影响心肌的病理生理学机制相同。我们对文献进行了综述,讨论了这种疾病的历史、特征性临床特征、过去使用的诊断标准以及这种疾病的推测病理生理学。
应激性心肌病是一种由严重情绪或身体应激引发的诊断不足的可逆性心肌病。它代表了一系列具有可逆性严重左心室收缩功能障碍的疾病,包括神经源性心肌病。它不限于日本人群,可影响任何种族背景或国籍的人。