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左三房心合并完全性肺静脉异位连接

Cor Triatriatum Sinister Associated with Total Anomalous Pulmonary Venous Connection.

机构信息

Perinatology Department, Ankara Etlik Zübeyde Hanım Women's Health, Training and Research Hospital, Ankara, Turkey.

Pediatric Cardiology Department, Ankara Etlik Zübeyde Hanım Women's Health, Training and Research Hospital, Ankara, Turkey.

出版信息

Z Geburtshilfe Neonatol. 2023 Aug;227(4):310-311. doi: 10.1055/a-2016-9440. Epub 2023 Aug 16.

Abstract

Cor triatriatum sinister is rare congenital heart disease. It is defined as the presence of an abnormal septum dividing the left atrium into two chambers, and in some cases may be associated with a total abnormal pulmonary venous connection. Prenatal diagnosis of cor triatriatum sinister may be possible with fetal echocardiography and the diagnosis can be made earlier than postnatal imaging techniques. In the fetal echocardiography performed in our patient, cor triatriatum sinister was present and the main pathology was the flow of right and left pulmonary vein return from the accessory atrium to the right atrium.

摘要

先天性三房心是一种罕见的心脏疾病。它的定义为异常隔膜将左心房分为两个腔室,在某些情况下可能与完全异常的肺静脉连接有关。胎儿超声心动图可能有助于先天性三房心的产前诊断,并且可以比产后影像学技术更早地做出诊断。在对我们的患者进行的胎儿超声心动图检查中,存在先天性三房心,主要病理学表现为左右肺静脉的血流从副心房回流到右心房。

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