巨大肺动脉动脉瘤伴轻度先天性肺狭窄

O. Başpınar, A. Irdem
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引用次数: 0

摘要

肺动脉动脉瘤是一种罕见的疾病。先天性瓣膜性肺动脉狭窄可发生狭窄后肺动脉扩张和动脉瘤。我们提出一个11岁的女孩转介到我们的诊所,由于心脏杂音检测的医生在评估背部疼痛。我们注意到轻度先天性肺狭窄和主肺动脉动脉瘤性扩张(肺动脉直径5.6 cm),并进行了肺球囊瓣膜成形术。继发于先天性瓣膜性肺狭窄的狭窄后动脉瘤扩张是一种罕见的临床现象。球囊瓣膜成形术是一种安全有效的治疗方法,如果没有肺动脉高压或先天性心脏病左向右分流。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant pulmonary artery aneurysm associated with mild congenital pulmonary stenosis
Pulmonary artery aneurysm is a rare condition. Poststenotic pulmonary artery dilatation and aneurysm may occur in congenital valvular pulmonary stenosis. We present an 11-year old girl referred to our clinic due to cardiac murmur detected by a physician during evaluation for back pain. We have noted mild congenital pulmonary stenosis and aneurysmatic dilatation of the main pulmonary artery (pulmonary artery diameter 5.6 cm) and performed pulmonary balloon valvuloplasty. Poststenotic aneurysmal dilatation secondary to congenital valvular pulmonary stenosis is a rare clinical entity. Balloon valvuloplasty is a safe and effective treatment method if there is no pulmonary hypertension or congenital heart disease with left-to-right shunt.
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