Bile duct size does not predict success of portoenterostomy for biliary atresia

被引:18
作者
Langenburg, SE [1 ]
Poulik, J [1 ]
Goretsky, M [1 ]
Klein, AA [1 ]
Klein, MD [1 ]
机构
[1] Childrens Hosp Michigan, Dept Pediat Gen & Thorac Surg, Detroit, MI 48202 USA
关键词
biliary atresia; Kasai procedure; portoenterostomy;
D O I
10.1053/jpsu.2000.6954
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background/Purpose: Presence of large bile ducts (>200 mu m) at the portal end-plate has been suggested to predict success after portoenterostomy. The authors reviewed their patients with biliary atresia to test the hypothesis that bile duct size in patients with successful portoenteroslomy was no different than in the patients with unsuccessful portoenterostomy. Methods: The authors reviewed the patients at their institution from 1989 to 1998 who had the diagnosis of biliary atresia (n = 38). A pathologist blinded to the results of the operation confirmed the measurements of the bile duct remnants. Results: Five of the 38 patients did not have a portoenterostomy. They underwent cholangiogram and liver biopsy and were evaluated for liver transplantation. All patients who underwent surgery(n = 33) had a Roux-en-y hepaticojejunostomy, Twenty-one patients had successful surgery (64%) and 12 patients (36%) had unsuccessful surgery. The average age at operation in the successful group was 50.9 +/- 3 days and in failures, 57.9 +/- 4 days (P = .16). Duct size at the portal end-plate was not different between the successes and failures. Two of the patients in the success group had no evidence of bile ducts grossly or histologically. Conclusion: Children presenting early in infancy (<3 months) with biliary atresia should undergo a portoenterostomy regardless of the size of the bile ducts at the time of exploration. Copyright (C) 2000 by W.B. Saunders Company.
引用
收藏
页码:1006 / 1007
页数:2
相关论文
共 19 条
[1]  
Altman RP, 1997, ANN SURG, V226, P348, DOI 10.1097/00000658-199709000-00014
[2]   Biliary atresia: Should all patients undergo a portoenterostomy? [J].
Azarow, KS ;
Phillips, MJ ;
Sandler, AD ;
Hagerstrand, I ;
Superina, RA .
JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (02) :168-174
[3]   Biliary atresia: Pathogenesis and treatment [J].
Bates, MD ;
Bucuvalas, JC ;
Alonso, MH ;
Ryckman, FC .
SEMINARS IN LIVER DISEASE, 1998, 18 (03) :281-293
[4]   LIVER-TRANSPLANTATION IN BABIES AND CHILDREN WITH EXTRAHEPATIC BILIARY ATRESIA [J].
BEATH, S ;
PEARMAIN, G ;
KELLY, D ;
MCMASTER, P ;
MAYER, A ;
BUCKELS, J .
JOURNAL OF PEDIATRIC SURGERY, 1993, 28 (08) :1044-1047
[5]   DUCTAL REMNANTS IN EXTRA-HEPATIC BILIARY ATRESIA - HISTOPATHOLOGIC STUDY WITH CLINICAL CORRELATION [J].
CHANDRA, RS ;
ALTMAN, RP .
JOURNAL OF PEDIATRICS, 1978, 93 (02) :196-200
[6]   100 CONSECUTIVE LIVER-TRANSPLANTS IN INFANTS AND CHILDREN - AN 8-YEAR EXPERIENCE [J].
ECKHOFF, DE ;
DALESSANDRO, AM ;
KNECHTLE, SJ ;
PIRSCH, JD ;
PLOEG, RJ ;
JUDD, RH ;
BELZER, FO ;
KALAYOGLU, M .
JOURNAL OF PEDIATRIC SURGERY, 1994, 29 (08) :1135-1140
[7]   BILIARY ATRESIA REGISTRY, 1976 TO 1989 [J].
KARRER, FM ;
LILLY, JR ;
STEWART, BA ;
HALL, RJ .
JOURNAL OF PEDIATRIC SURGERY, 1990, 25 (10) :1076-1081
[8]   LONG-TERM OUTCOME AFTER SURGERY FOR BILIARY ATRESIA - STUDY OF 40 PATIENTS SURVIVING FOR MORE THAN 10 YEARS [J].
LAURENT, J ;
GAUTHIER, F ;
BERNARD, O ;
HADCHOUEL, M ;
ODIEVRE, M ;
VALAYER, J ;
ALAGILLE, D .
GASTROENTEROLOGY, 1990, 99 (06) :1793-1797
[9]   THE EFFICACY OF KASAI OPERATION FOR BILIARY ATRESIA - A SINGLE INSTITUTIONAL EXPERIENCE [J].
LIN, JN ;
WANG, KL ;
CHUANG, JH .
JOURNAL OF PEDIATRIC SURGERY, 1992, 27 (06) :704-706
[10]  
LYNCH SV, 1992, TRANSPLANT P, V24, P186