Literature DB >> 25840084

The classification based on intrahepatic portal system for congenital portosystemic shunts.

Hiroyuki Kanazawa1, Shunsuke Nosaka2, Osamu Miyazaki2, Seisuke Sakamoto3, Akinari Fukuda3, Takanobu Shigeta3, Atsuko Nakazawa4, Mureo Kasahara3.   

Abstract

BACKGROUND/
PURPOSE: Liver transplantation was previously indicated as a curative operation for congenital absence of portal vein. Recent advances in radiological interventional techniques can precisely visualize the architecture of the intrahepatic portal system (IHPS). Therefore, the therapeutic approach for congenital portosystemic shunt (CPS) needs to be reevaluated from a viewpoint of radiological appearances. The aim of this study was to propose the IHPS classification which could explain the pathophysiological characteristics and play a complementary role of a therapeutic approach and management for CPS.
METHODS: Nineteen patients with CPS were retrospectively reviewed. The median age at diagnosis was 6.8 years old. Eighteen of these patients underwent angiography with a shunt occlusion test and were classified based of the severity of the hypoplasia of IHPS.
RESULTS: The eighteen cases who could undergo the shunt occlusion test were classified into mild (n=7), moderate (n=6) and severe types (n=5) according to the IHPS classification. The IHPS classification correlated with the portal venous pressure under shunt occlusion, the histopathological findings, postoperative portal venous flow and liver regeneration. Shunt closure resulted in dramatic improvement in the laboratory data and subclinical encephalopathy. Two patients with the severe type suffered from sepsis associated with portal hypertension after treatment, and from the portal flow steal phenomenon because of the development of unexpected collateral vessels. The patients with the severe type had a high risk of postoperative complications after shunt closure in one step, even if the PVP was relatively low during the shunt occlusion test.
CONCLUSION: The IHPS could be visualized by the shunt occlusion test. The IHPS classification reflected the clinicopathological features of CPS, and was useful to determine the therapeutic approach and management for CPS.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Abernethy malformation; Congenital absence of the portal vein; Congenital portosystemic shunt; Liver transplantation; Shunt occlusion test

Mesh:

Year:  2015        PMID: 25840084     DOI: 10.1016/j.jpedsurg.2015.01.009

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  19 in total

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2.  Congenital absence of the portal vein: Define the portosystemic shunt, avoid liver transplantation.

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6.  Interventional embolization of congenital intrahepatic shunts in children.

Authors:  Lin Wu; Lu Zhao; Ying Lu; Lan He; Xihong Hu
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Review 7.  Abernethy malformation: Single-center experience from India with review of literature.

Authors:  Swapnil Sharma; Prashant R Bobhate; Shailesh Sable; Suneed Kumar; Kapildev Yadav; Sharad Maheshwari; Saista Amin; Ashutosh Chauhan; Vibha Varma; Sorabh Kapoor; Vinay Kumaran
Journal:  Indian J Gastroenterol       Date:  2018-09-05

8.  Understanding the Pathophysiology of Portosystemic Shunt by Simulation Using an Electric Circuit.

Authors:  Moonhwan Kim; Keon-Young Lee
Journal:  Biomed Res Int       Date:  2016-10-27       Impact factor: 3.411

Review 9.  Congenital portosystemic venous shunt.

Authors:  M Papamichail; M Pizanias; N Heaton
Journal:  Eur J Pediatr       Date:  2017-12-14       Impact factor: 3.183

10.  Role of ultrasonography in early diagnosis of congenital extrahepatic portosystemic shunt.

Authors:  Kithir Mohamed Anwer Sadat
Journal:  BJR Case Rep       Date:  2016-05-25
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