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首页> 外文期刊>Pediatric radiology >Coil embolization of a congenital intrahepatic arterioportal fistula: increasing experience in management.
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Coil embolization of a congenital intrahepatic arterioportal fistula: increasing experience in management.

机译:先天性肝内门静脉瘘的线圈栓塞术:增加管理经验。

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摘要

Congenital intrahepatic arterioportal fistula (IAPF) is a rare condition and there is limited experience of transcatheter embolization. We report here the transcatheter coil embolization of an incidentally found, asymptomatic congenital IAPF in a 16-month-old patient. After demonstrating that the IAPF was fed by two branches of a dilated left hepatic artery and drained into an aneurysm of the left portal vein, the feeding arteries were superselectively catheterized and occluded by microcoils in a single session. Follow-up was uneventful for 1 year. With respect to this and previously reported cases, we believe that embolization of feeding arteries is a safe and effective method that should be the primary choice of treatment; however, further cases should be reported to confirm this belief.
机译:先天性肝内动静脉瘘(IAPF)是一种罕见病,经导管栓塞的经验有限。我们在此报告了一名16个月大患者中偶然发现的无症状先天性IAPF的经导管线圈栓塞术。在证明IAPF由扩张的左肝动脉的两个分支供血并排入左门静脉的动脉瘤后,对供血动脉进行了超选择性导管插入,并在单个疗程中被微线圈阻塞。随访1年无病。对于这种情况和先前报道的病例,我们认为栓塞动脉是一种安全有效的方法,应该是治疗的主要选择。但是,应报告更多病例以证实这一信念。

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