Literature DB >> 1593379

Successful late Kasai portoenterostomy.

A Bielamowicz1, J J Weitzman, N S Alshak, P Rosenthal.   

Abstract

This article describes an infant with extrahepatic biliary atresia who underwent a successful hepatoportoenterostomy at age 132 days in spite of a delay in diagnosis. Contributing to the delay in diagnosis of this case were the lack of appreciation of alcoholic stools, the presence of a gallbladder and distal common bile duct on ultrasound examination, and insufficient biopsy material for interpretation. This case emphasizes the variability in presentation and potential difficulties in diagnosis and the need for intraoperative cholangiogram and exploratory laparotomy in such cases. An approach to the patient with extrahepatic biliary atresia who is diagnosed late is discussed. A successful outcome can be achieved for such patients.

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Year:  1992        PMID: 1593379     DOI: 10.1097/00005176-199202000-00020

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  2 in total

1.  A multicenter study of primary liver transplantation for biliary atresia in Japan.

Authors:  Keiichi Uto; Yukihiro Inomata; Seisuke Sakamoto; Taizo Hibi; Hideyuki Sasaki; Masaki Nio
Journal:  Pediatr Surg Int       Date:  2019-09-18       Impact factor: 1.827

2.  Clinical and pathological challenges in the diagnosis of late-onset biliary atresia: four case studies.

Authors:  J P U Fontenele; A A Schenka; G Hessel; V M Jarry; C A F Escanhoela
Journal:  Braz J Med Biol Res       Date:  2016-02-02       Impact factor: 2.590

  2 in total

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