LV Diverticulum with Concurrent Takotsubo Cardiomyopathy

John Raper
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Abstract

Introduction Left ventricular diverticulum was first described in 1838 and is thought to occur in 0.4% of the population [1,2]. Left ventricular diverticulum is challenging to diagnose due to the asymptomatic nature and lack of consistent ways to describe the outpouching, however it is known that it contains all layers of the heart [3-5]. Previous authors have tried to classify based on using the size of diverticulum compared to the size of the left ventricle [4]. Diverticulum can be classified as either muscular or fibrous and they display contractile features consistent with the remaining heart [3,4]. As much as 30% of left diverticulum cases are not associated with congenital abnormalities and can present with chest pain [3]. Echocardiography and angiography can be used for diagnosis and surgical resection are typically the treatment of choice before complications such as endocarditis, arrhythmia, heart failure, and tamponade occur [1,6].
左室憩室并发Takotsubo心肌病
左室憩室于1838年首次被描述,被认为发生在0.4%的人群中[1,2]。由于左室憩室无症状且缺乏一致的方法来描述其流出,因此诊断左室憩室具有挑战性,但已知它包含心脏的所有层[3-5]。以前的作者试图根据憩室的大小与左心室的大小进行分类。憩室可分为肌性和纤维性两种,它们表现出与剩余心脏一致的收缩特征[3,4]。多达30%的左憩室病例与先天性异常无关,可表现为胸痛。超声心动图和血管造影可用于诊断,手术切除是在发生心内膜炎、心律失常、心力衰竭和心包填塞等并发症之前的典型治疗选择[1,6]。
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