Lutembacher’s Syndrome in a young female treated Surgically: A Case Report

Sultan Sarwar Parvez, S. Gupta, Reazul Haque, J. Uddin
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Abstract

Lutembacher’s syndrome is a rare clinical condition presenting with a combination of congenital atrial septal defect (ASD) and acquired mitral stenosis (MS). Lutembacher’s syndrome is more prevalent in developing countries and its prevalence depends on the prevalence of rheumatic fever in that geographical area. The syndrome can present at any age but is usually more commonly observed in young female adults. Echocardiography remains the gold standard for diagnosis and evaluation of Lutembacher’s syndrome (LS). Now a days many treatment options are available for LS – either percutaneous intervention or surgical correction. But pericardial patch closure of atrial septal defect and prosthetic mitral valve replacement is the treatment of choice for Lutembacher’s syndrome. Bangladesh Heart Journal 2022; 37(2): 143-147
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手术治疗年轻女性Lutembacher综合征一例报告
Lutembacher综合征是一种罕见的临床病症,表现为先天性房间隔缺损(ASD)和获得性二尖瓣狭窄(MS)的结合。Lutembacher综合征在发展中国家更为普遍,其流行程度取决于该地理区域风湿热的流行程度。这种综合征可以出现在任何年龄,但通常更常见于年轻的成年女性。超声心动图仍然是诊断和评估Lutembacher综合征(LS)的金标准。现在有许多治疗方法可供选择,要么经皮介入治疗,要么手术矫正。但心包补片封闭房间隔缺损和人工二尖瓣置换术是治疗Lutembacher综合征的首选方法。孟加拉国心脏杂志2022;37 (2): 143 - 147
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