Division of Interventional Radiology, H-3646, Stanford University Medical Center, 300 Pasteur Drive, Stanford, CA 94305-5642, USA.
J Vasc Interv Radiol. 2011 Aug;22(8):1199-205. doi: 10.1016/j.jvir.2011.01.438.
Patients with autogenous native vessel portosystemic shunts, whether surgical or congenital, may experience complications of excess shunt flow, including hepatopulmonary syndrome (HPS), hepatic encephalopathy (HE), and hepatic insufficiency. The authors explored endovascular reduction or occlusion of autogenous portosystemic shunts using methods commonly employed in transjugular intrahepatic portosystemic shunt (TIPS) reduction in four pediatric patients. Before treatment, the patients had hypoplastic, atrophic, or thrombosed portal veins. Following intervention, symptoms of overshunting resolved or improved in all patients without major complications. The innate plasticity of the pediatric portal venous system allowed for hypertrophy or development and maturation of cavernous transformations to accommodate increased hepatopetal blood flow and pressure.
自体原生门静脉-体循环分流的患者,无论是手术性还是先天性,可能会出现分流过度的并发症,包括肝肺综合征(HPS)、肝性脑病(HE)和肝功能不全。作者探索了使用经颈静脉肝内门体分流术(TIPS)减少术常见的方法对 4 例儿科患者的自体门体分流进行血管内减少或闭塞。治疗前,患者的门静脉发育不良、萎缩或血栓形成。干预后,所有患者的分流过度症状均得到缓解或改善,无重大并发症。儿童门静脉系统的固有可塑性允许海绵体转化的肥大或发育和成熟,以适应增加的肝向血流和压力。