Biliary atresia

Semin Pediatr Surg. 2000 Nov;9(4):177-86. doi: 10.1053/spsu.2000.18846.

Abstract

Although the prognosis of biliary atresia has been dramatically improved in the era of liver transplantation, the Kasai operation is still the first line of surgical treatment. Successful hepatic portoenterostomy depends on early diagnosis and surgery, adequate surgical technique, prevention of cholangitis, and precise postoperative management.

Publication types

  • Review

MeSH terms

  • Biliary Atresia / diagnosis
  • Biliary Atresia / etiology
  • Biliary Atresia / pathology
  • Biliary Atresia / surgery*
  • Child
  • Cholangitis / etiology
  • Humans
  • Portoenterostomy, Hepatic* / adverse effects
  • Reoperation