Membranous ventricular septal aneurysms are a rare condition with most being asymptomatic in nature though can have symptoms of arrhythmia, thrombosis or more rarely outflow tract obstruction.Reference Carcano, Kanne and Kirsch1 A 40-year-old female with trisomy 18 and unrepaired ventricular septal defect was referred to our centre because transthoracic echocardiography showed severe right ventricular outflow obstruction. Her large inlet ventricular septal defect extended into the perimembranous septum. The enormous aneurysmal tricuspid valve tissue not only closed off the ventricular septal defect with no residual shunt but also extended into the right ventricular outflow tract causing severe obstruction. Clinically she remained asymptomatic. She had past medical history of developmental delay, brain cyst and hypertension. Cardiac catheterisation showed severely elevated right ventricular systolic pressure (98 mmHg) with a gradient of 70 mmHg to the pulmonary artery. Pulmonary vascular resistance was 3 Woods Units. Transthoracic and intracardiac echocardiography showed to and fro flow through the ventricular septal defect from left ventricle to the blind pouch created by the membranous ventricular septal aneurysm (Fig 1, Video). This aneurysm crossed the pulmonary valve in systole and caused severe right ventricular outflow obstruction. Angiography in the left and right ventricles showed a large membranous ventricular septal aneurysm which caused dynamic obstruction in the right ventricular outflow obstruction (Fig 2). She was then referred for surgical repair.
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