Literature DB >> 32791304

Surgical ligation of a portosystemic shunt for the treatment of type II Abernethy malformation in 12 children.

Jin-Shan Zhang1, Long Li2.   

Abstract

OBJECTIVE: This study aimed to investigate the feasibility and effectiveness of surgical ligation in the treatment of a congenital extrahepatic portosystemic shunt (Abernethy malformation) in children.
METHODS: Twelve children (aged 10 days to 13.3 years; six boys and six girls) with Abernethy malformation were admitted to the Capital Institute of Pediatrics (Beijing, China) from May 2014 to November 2019 owing to hyperammonemia. Among them, nine suffered from hematochezia, two had elevated liver transaminase levels or jaundice, and one had hypoxemia. Their surgical procedures and outcomes were retrospectively analyzed. Portal pressure measurement and angiography of the portal vein were performed before and after the occlusion of the portosystemic shunt during the surgery. Six patients underwent a single-stage ligation of the portosystemic shunt, five underwent a two-stage ligation of the portosystemic shunt, and one was treated with a partial ligation of the portosystemic shunt.
RESULTS: Each of the operations was successfully completed with an operative time ranging from 60 to 240 minutes and with an intraoperative blood loss ranging from 50 to 200 mL. Three children had a blood transfusion. The postoperative portal pressure was significantly higher than that before the surgery in all children. The patients were followed for 5 to 70 months. The symptoms of hematochezia were relieved in nine patients after the surgery. The levels of blood bilirubin and transaminase returned to normal after the surgery in two patients. The oxygen saturation returned to normal in one patient. The level of blood ammonia was normal after the surgery in all patients.
CONCLUSIONS: The surgical ligation of the portosystemic shunt was an effective method to treat a type II Abernethy malformation. According to the portal pressure after the occlusion of the portosystemic shunt, a single or staged procedure was selected.
Copyright © 2020 Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Abernethy malformation; Children; Congenital portosystemic shunt; Ligation; Surgery

Mesh:

Year:  2020        PMID: 32791304     DOI: 10.1016/j.jvsv.2020.08.001

Source DB:  PubMed          Journal:  J Vasc Surg Venous Lymphat Disord


  3 in total

1.  Percutaneous treatment of a huge patent ductus venosus and severe portal vein hypoplasia using a Figulla Flex II atrial septal defect occluder in a 2-year-old infant: a case report.

Authors:  Marek Kardos; Erwin Kitzmueller; Peter Olejnik; Ina Michel-Behnke
Journal:  Eur Heart J Case Rep       Date:  2021-11-11

2.  A rare presentation of type II Abernethy malformation and nephrotic syndrome: Case report and review.

Authors:  Xin Wu; Weizhong Gu; Yongzhi Lin; Lina Ye
Journal:  Open Life Sci       Date:  2022-07-21       Impact factor: 1.311

3.  Case report: Rare abernethy malformation with hepatopulmonary syndrome in a pediatric patient.

Authors:  Lianfu Ji; Zhaoming Ji; Dandan Xiang; Yuming Qin; Shiwei Yang
Journal:  Front Pediatr       Date:  2022-09-09       Impact factor: 3.569

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.