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婴儿高流量先天性肝内动脉-门静脉畸形的经导管栓塞术

Transcatheter embolization of a high-flow congenital intrahepatic arterial-portal venous malformation in an infant.

作者信息

Routh W D, Keller F S, Cain W S, Royal S A

机构信息

Department of Radiology, University of Alabama, Birmingham.

出版信息

J Pediatr Surg. 1992 Apr;27(4):511-4. doi: 10.1016/0022-3468(92)90350-g.

Abstract

An intrahepatic arterial-portal venous malformation (APVM) was diagnosed in a 4 1/2-month-old infant with portal hypertension. Visceral angiography showed a large saccular vascular space in the left hepatic lobe with a multiplicity of feeding arteries and drainage into the left portal vein. The lesion was successfully treated by transcatheter embolization following two unsuccessful surgical procedures. Two years later portal vein thrombosis with cavernous transformation was diagnosed, possibly a consequence of the high-flow arterial-portal shunt and its subsequent occlusion. Knowledge of the anatomic differences between this rare congenital APVM and the more commonly occurring arterial-portal fistula is crucial in planning effective transcatheter embolotherapy or surgery for these lesions.

摘要

一名4个半月大、患有门静脉高压症的婴儿被诊断出患有肝内动静脉畸形(APVM)。内脏血管造影显示左肝叶有一个大的囊状血管腔,有多个供血动脉,并引流至左门静脉。在两次手术失败后,通过经导管栓塞术成功治疗了该病变。两年后,诊断出伴有海绵样变性的门静脉血栓形成,这可能是高流量动静脉分流及其随后闭塞的结果。了解这种罕见的先天性APVM与更常见的动静脉瘘之间的解剖学差异,对于为这些病变规划有效的经导管栓塞治疗或手术至关重要。

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