Literature DB >> 1345477

Biliary atresia.

R Ohi1, M Ibrahim.   

Abstract

Although biliary atresia is characterized by luminal obstruction of the extrahepatic bile ducts, the etiology and the pathophysiology of the liver are still controversial. The prognosis of biliary atresia has been improved after the introduction of Kasai's hepatic portoenterostomy, but there are still many problems to be solved in the treatment of this disease. Successful results of hepatic portoenterostomy depend on early diagnosis and operation, adequate operative technique, prevention of postoperative cholangitis, and precise postoperative management. However, we are on the verge of a new era in the therapy of biliary atresia combining portoenterostomy with liver transplantation.

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Mesh:

Year:  1992        PMID: 1345477

Source DB:  PubMed          Journal:  Semin Pediatr Surg        ISSN: 1055-8586            Impact factor:   2.754


  11 in total

Review 1.  Effects of age at Kasai portoenterostomy on the surgical outcome: a review of the literature.

Authors:  Masaki Nio; Motoshi Wada; Hideyuki Sasaki; Hiromu Tanaka
Journal:  Surg Today       Date:  2014-09-12       Impact factor: 2.549

2.  The morphological and histopathological assessment of Alagille syndrome with extrahepatic bile duct obstruction: the importance of the differential diagnosis with subgroup "o" biliary atresia.

Authors:  Masahiro Takeda; Seisuke Sakamoto; Hajime Uchida; Seiichi Shimizu; Yusuke Yanagi; Akinari Fukuda; Takako Yoshioka; Mureo Kasahara
Journal:  Pediatr Surg Int       Date:  2021-06-02       Impact factor: 1.827

3.  The effect of hepatic portal dissection on the portal vein structure in biliary atresia.

Authors:  R Ohi; Y Hayashi; N Endo; M Ibrahim; M Nio; M Goto; D Iwami
Journal:  Surg Today       Date:  1994       Impact factor: 2.549

4.  The porta hepatis microcyst: an additional sonographic sign for the diagnosis of biliary atresia.

Authors:  Mériam Koob; Danièle Pariente; Dalila Habes; Béatrice Ducot; Catherine Adamsbaum; Stéphanie Franchi-Abella
Journal:  Eur Radiol       Date:  2016-08-23       Impact factor: 5.315

Review 5.  Medical management of chronic liver diseases (CLD) in children (part II): focus on the complications of CLD, and CLD that require special considerations.

Authors:  Mortada H F El-Shabrawi; Naglaa M Kamal
Journal:  Paediatr Drugs       Date:  2011-12-01       Impact factor: 3.022

6.  Orthotopic liver transplantation for congenital biliary atresia. An 11-year, single-center experience.

Authors:  J A Goss; C R Shackleton; K Swenson; N L Satou; B J Nuesse; D K Imagawa; M M Kinkhabwala; P Seu; J S Markowitz; S M Rudich; S V McDiarmid; R W Busuttil
Journal:  Ann Surg       Date:  1996-09       Impact factor: 12.969

7.  A morphological study of the removed livers from patients receiving living donor liver transplantation for adult biliary atresia.

Authors:  Toshiharu Matsuura; Kenichi Kohashi; Yusuke Yanagi; Isamu Saeki; Makoto Hayashida; Shinichi Aishima; Yoshinao Oda; Tomoaki Taguchi
Journal:  Pediatr Surg Int       Date:  2012-10-12       Impact factor: 1.827

8.  Liver transplantation().

Authors:  M Rossi; G Mennini; Q Lai; S Ginanni Corradini; F M Drudi; F Pugliese; P B Berloco
Journal:  J Ultrasound       Date:  2007-04-16

9.  Maternal microchimerism in the livers of patients with biliary atresia.

Authors:  David L Suskind; Philip Rosenthal; Melvin B Heyman; Denice Kong; Greg Magrane; Lee-Ann Baxter-Lowe; Marcus O Muench
Journal:  BMC Gastroenterol       Date:  2004-07-31       Impact factor: 3.067

Review 10.  The Sea Lamprey as an Etiological Model for Biliary Atresia.

Authors:  Yu-Wen Chung-Davidson; Chu-Yin Yeh; Weiming Li
Journal:  Biomed Res Int       Date:  2015-05-26       Impact factor: 3.411

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