Enormous Enlargement of Right Atrium Occurred Late After Surgical Dilation of Pulmonary Valve Stenosis: Case Report.

Hanane Zouzou
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Abstract

Congenital pulmonary valve stenosis is a relatively common congenital defect, often related to abnormal development and fusion of pulmonary valves. Critical pulmonary valve stenosis should be treated, early in life, before dilation of right chambers, and occurrence of arrhythmias. We report one case of enormous enlargement of right atrium revealed by typical atrial flutter which occurred very late, in 48-year-old man, who underwent surgical dilation of pulmonary valve stenosis at eleven years old, but without repairing dilated tricuspid annulus. Despite successfully ablation of atrial flutter in our cathlab, the patient developed atrial fibrillation, because of an enormous enlargement of right atrium and massive tricuspid regurgitation.
肺动脉瓣狭窄手术扩张后晚期出现右心房巨大增大:病例报告。
先天性肺动脉瓣狭窄是一种比较常见的先天性缺陷,通常与肺动脉瓣的发育和融合异常有关。危重的肺动脉瓣狭窄应在生命早期进行治疗,以避免右心房扩张和心律失常的发生。我们报告了一例右心房巨大增大并伴有典型心房扑动的病例,该患者 48 岁,在 11 岁时接受了肺动脉瓣狭窄的手术扩张,但没有修复扩张的三尖瓣环。
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