Rare congenital fistula connection between right subclavian artery and superior vena cava presenting in neonate with congestive cardiac failure

Awadh Salem Al-Majrafi, Naela Khalifa Al Kalbani, Farida Ambusaidi
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Abstract

Intra-thoracic arteriovenous malformations are uncommon. As the most reported localizations of AVM are the head (vein of Galen malformation), the abdomen (infantile hepatic hemangioma), the neck and extremities.1 Arterio venous malformation divided into congenital and acquired. The congenital forms are even more uncommon and patients present with variable symptoms that make the diagnosis more challenging.2,3 A congenital Aortocaval fistula from subclavian artery to the superior vena cava (SVC) may represent a subclass of this condition.
新生儿充血性心力衰竭的罕见先天性瘘管连接右锁骨下动脉与上腔静脉
胸腔内动静脉畸形并不常见。AVM的报告最多的部位是头部(Galen畸形的静脉)、腹部(婴儿肝血管瘤)、颈部和四肢。1动静脉畸形分为先天性和获得性。先天性形式更为罕见,患者表现出的各种症状使诊断更具挑战性。2,3从锁骨下动脉到上腔静脉(SVC)的先天性主动脉腔瘘可能代表这种疾病的一个亚类。
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