Kudo Shohei, Onozawa Shiro, Miyauchi Ryosuke, Matsuki Ryota, Sakamoto Yoshihiro
Department of Hepato-Biliary-Pancreatic Surgery Kyorin University Hospital Mitaka Japan.
Department of Radiology Kyorin University Hospital Mitaka Japan.
Ann Gastroenterol Surg. 2025 May 20;9(5):1104-1108. doi: 10.1002/ags3.70043. eCollection 2025 Sep.
Patent ductus venosus is a congenital portosystemic shunt that may cause progressive portal hypertension, hepatic encephalopathy, and focal nodular hyperplasia of the liver. Embolization of the Arantius' duct is the first choice of treatment in infants and children. However, it carries the risk of coil migration into the systemic circulation in adult patients with larger Arantius ducts. Additionally, the primary closure of the Arantius' duct may result in acute portal hypertension. Herein, we present a two-stage treatment for adult patent large ductus venosus (Arantius' duct). A 23-year-old female patient with hypoalbuminemia showed a patent large Arantius' duct (diameter = 45 mm), intrahepatic portal venous hypoplasia, and multiple hepatic nodules with dynamic computed tomography (CT). Preoperative angiography showed the absence of the intrahepatic portal vein, and tentative occlusion of the Arantius' duct increased the portal pressure from 9 to 15 mmHg with visualization of only a few portal branches. Therefore, we conducted a two-stage treatment for the Arantius' duct. In the first stage, we used an open approach to perform angioplasty of the Arantius' duct to reduce the size from 45 to 8 mm in diameter, which gradually increased the intrahepatic portal blood flow in the follow-up CT scan. The second-stage embolization of the Arantius' duct was performed using an interventional procedure via the internal jugular vein 4 months after the first stage. The patient's recovery was uneventful, and post-treatment CT showed increased intrahepatic portal flow. Serum albumin value increased from 2.7 to 3.7 g/dL 2 weeks post-treatment.
静脉导管未闭是一种先天性门体分流,可导致进行性门静脉高压、肝性脑病和肝脏局灶性结节性增生。动脉导管栓塞术是婴幼儿的首选治疗方法。然而,对于动脉导管较大的成年患者,存在线圈迁移至体循环的风险。此外,动脉导管的直接闭合可能导致急性门静脉高压。在此,我们介绍一种针对成年人大静脉导管未闭(动脉导管)的两阶段治疗方法。一名23岁的低白蛋白血症女性患者,动态计算机断层扫描(CT)显示动脉导管粗大(直径 = 45 mm)、肝内门静脉发育不全以及多个肝结节。术前血管造影显示肝内门静脉缺如,临时闭塞动脉导管使门静脉压力从9 mmHg升至15 mmHg,仅可见少数门静脉分支。因此,我们对动脉导管进行了两阶段治疗。在第一阶段,我们采用开放手术对动脉导管进行血管成形术,将其直径从45 mm缩小至8 mm,在后续CT扫描中肝内门静脉血流逐渐增加。第一阶段4个月后,通过颈内静脉采用介入方法进行了动脉导管的第二阶段栓塞。患者恢复顺利,治疗后CT显示肝内门静脉血流增加。治疗后2周,血清白蛋白值从2.7 g/dL升至3.7 g/dL。