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首页> 外文期刊>The Internet Journal of Thoracic and Cardiovascular Surgery >Cor triatriatum sinistrum: a rare congenital cardiac anomaly presenting in an elderly man with coronary artery disease
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Cor triatriatum sinistrum: a rare congenital cardiac anomaly presenting in an elderly man with coronary artery disease

机译:Cor triatriatum sinistrum:一种患有冠心病的老人中罕见的先天性心脏异常

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Cor triatriatum sinistrum is a rare congenital cardiac anomaly in which a fibromuscular membrane divides the left atrium. We describe a case of cor triatriatum sinistrum: a rare congenital cardiac anomaly presenting in an elderly man with coronary artery disease.Diagnosis is usually achieved by echocardiography, therapy of choice is excision of the membrane. Introduction Cor triatriatum sinister is a rare congenital defect in which the left atrium is divided by a fibromuscular membrane into two distinct chambers[1]. Divided left atrium or Cor Triatriatum, is a congenital cardiac malformation having low incidence during paediatric age, ranging between 0.1 - 0.4%. Its appearance in adulthood is even more exceptional and often inadvertently discovered[2]. It is usual for patients to present in infancy and early childhood, although some cases remain undetected until adult life. As a consequence of trans-membrane flow obstruction, the clinical features often mimic mitral stenosis. At present, the reasons for late presentation are poorly understood[3]. Severity of the disease depends on the size of the opening on the membrane[4]. Case Presentation Our case was a 55 years old man and he was examined at an other institution for dyspnea and increasing fatigue. He was in New York Heart Association (NYHA) functional class III at presentation.He was evaluated by clinical,hematological,electrocardiographical and echocardiographical examination preoperatively. Transthoracic echocardiography(TTE) showed mild mitral regurgitation. Diameter of left atrium(57mm) and left ventricle(54/37mm)were widened.Left ventricular EF was 50%. Echocardiographic score was found to be 9. Other valves’ functions were normal. Because he was middle-aged, coronary arteriography(CAG) and cardiac catheterization were performed. CAG showed significant stenotic lesions in LAD and CxOM1 branch. It confirmed mild mitral regurgitation(Figures 1&2).
机译:三角肌Coristrrum是一种罕见的先天性心脏异常,其中纤维肌膜将左心房分开。我们描述了一个三头肌窦性鼻窦炎病例:老年冠心病的罕见先天性心脏异常。诊断通常是通过超声心动图进行的,选择的治疗方法是切除膜。引言Triatriatum sinister是一种罕见的先天性缺陷,左心房被纤维肌膜分为两个不同的腔室[1]。先天性心脏畸形是左心房或心房颤动,在小儿时期发病率低,在0.1%至0.4%之间。它在成年期的外观更为特殊,并且经常被无意中发现[2]。患者通常在婴儿期和儿童早期就诊,尽管有些病例直到成年才被发现。由于跨膜血流阻塞,其临床特征通常模仿二尖瓣狭窄。目前,迟发的原因尚不清楚[3]。疾病的严重程度取决于膜上开口的大小[4]。病例介绍我们的病例是一个55岁的男人,他在另一家机构接受了呼吸困难和疲劳加剧检查。演讲时他处于纽约心脏协会(NYHA)的III级功能。术前已通过临床,血液学,心电图和超声心动图检查对他进行了评估。经胸超声心动图(TTE)显示轻度二尖瓣反流。左心房(57mm)和左心室(54 / 37mm)的直径扩大了,左心室EF为50%。超声心动图评分为9。其他瓣膜功能正常。由于他是中年,因此进行了冠状动脉造影(CAG)和心脏导管插入术。 CAG在LAD和CxOM1分支中显示出明显的狭窄病变。它证实了轻度二尖瓣关闭不全(图1和图2)。

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