Literature DB >> 22617089

The role of liver transplantation for congenital extrahepatic portosystemic shunt.

Seisuke Sakamoto1, Takanobu Shigeta, Akinari Fukuda, Hideaki Tanaka, Atsuko Nakazawa, Shunsuke Nosaka, Shinji Uemoto, Mureo Kasahara.   

Abstract

BACKGROUND: Congenital extrahepatic portosystemic shunt (CEPS) is reported more frequently because of advances in imaging techniques. Liver transplantation (LT) is a therapeutic option, although the indications for LT are still controversial.
METHODS: This study reviewed 34 cases of LT for CEPS, including 30 cases reported in the English medical literature and the patients treated in our department, to collect the clinical data associated with LT.
RESULTS: The median age at diagnosis and LT was 3.7 and 6.8 years, respectively. Hepatic encephalopathy, including persistent hyperammonemia, was the most common indication of LT. Pulmonary complications, including hepatopulmonary syndrome and pulmonary hypertension, were the second most common indications of LT, and those patients underwent LT soon after the diagnosis. Although a shunt directly draining into the inferior vena cava was the most common type and managed by a simple direct anastomosis of the portal vein at LT, some cases required the modification of the portal vein reconstruction, such as interposition. Thirty patients were alive with a median follow-up period of 18 months.
CONCLUSIONS: LT for CEPS showed an excellent outcome. The development of pulmonary complications is an early indication for LT. Precise planning of portal vein reconstruction is required before LT.

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Year:  2012        PMID: 22617089     DOI: 10.1097/TP.0b013e318250c157

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  8 in total

1.  Ductal paucity and Warkany syndrome in a patient with congenital extrahepatic portocaval shunt.

Authors:  Vikrant Sood; Rajeev Khanna; Seema Alam; Dinesh Rawat; Shorav Bhatnagar; Archana Rastogi
Journal:  World J Hepatol       Date:  2014-05-27

2.  Pre and postnatal diagnosis of congenital portosystemic shunt: Impact of interventional therapy.

Authors:  Shireen Mreish; Mohamed A Hamdan
Journal:  Int J Pediatr Adolesc Med       Date:  2019-03-15

Review 3.  Congenital extrahepatic portosystemic shunt: description of four cases and review of the literature.

Authors:  Francesca Romana Ponziani; Mariella Faccia; Maria Assunta Zocco; Valerio Giannelli; Adriano Pellicelli; Giuseppe Maria Ettorre; Nicoletta De Matthaeis; Fabrizio Pizzolante; Anna Maria De Gaetano; Laura Riccardi; Maurizio Pompili; Gian Ludovico Rapaccini
Journal:  J Ultrasound       Date:  2018-10-24

4.  Clinical characteristics and therapeutic outcomes of pulmonary arterial hypertension secondary to congenital portosystemic shunts.

Authors:  Jinjin Wu; Yi Lu; Wenzhuo Zhao; Jie Shen; Fen Li; Hao Zhang; Qimin Chen; Lijun Fu
Journal:  Eur J Pediatr       Date:  2020-10-03       Impact factor: 3.183

5.  A 10-year-old boy with dyspnea and hypoxia: abernathy malformation masquerading as pulmonary arteriovenous fistula.

Authors:  Lijian Xie; Yun Li; Xunwei Jiang; Jian Zhao; Tingting Xiao
Journal:  BMC Pediatr       Date:  2019-02-11       Impact factor: 2.125

6.  Living-donor liver transplantation for Abernethy malformation - case report and review of literature.

Authors:  Hoang Duc Nam
Journal:  Ann Hepatobiliary Pancreat Surg       Date:  2020-05-31

Review 7.  Congenital portosystemic venous shunt.

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

8.  Abernethy malformation: beware in cases of unexplained hepatic encephalopathy in adults-case report and review of the relevant literature.

Authors:  Romeu Duarte Mesquita; Marta Sousa; Filipa Vilaverde; Rosa Cardoso
Journal:  BJR Case Rep       Date:  2017-11-16
  8 in total

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