Abstract
Intrahepatic bile ducts are patent in the liver of patients with biliary atresia in early infancy. Small bile ducts at the porta hepatis continuing to the intrahepatic ducts usually terminate in fibrous tissue replacing the hepatic radicles, which does not extend to the common hepatic duct. Therefore, the level of transection of the fibrous tissue at the porta hepatis is of prime importance for successful hepatic portoenterostomy. Transection should be done at the level of the posterior surface of the portal vein. The overall cure rate of surgery for biliary atresia was 30%. In our recent series, however, the results have markedly improved and the cure rate has been increased to 55%. There are 47 patients living without jaundice, 22 of them for more than 5 years. The longest survivors are 23 years old. All the longterm survivors are leading a normal life for their age, although 6 of them have some physical or mental handicap. Early operation, adequate surgical technique, and prevention of postoperative cholangitis are requisites for successful hepatic portoenterostomy.
Résumé
Chez les nouveaux-nés atteints d'atrésie biliaire, les canaux biliaires intra-hépatiques sont perméables. Dans le hile hépatique, ces canaux intrahépatiques se terminent par de fins canalicules enserrés dans du tissu fibreux, qui ne se poursuivent pas jusqu'au canal hépatique commun. Le niveau de section du tissu fibreux dans le hile hépatique est donc très important pour le succès de l'hépaticoentérostomie. Cette section doit être faite au niveau de la face postérieure de la veine porte. La chirurgie pour atrésie biliaire donnait 30% de guérisons. Dans notre récente série, les résultats ont été améliorés jusqu'à 55% de guérisons. Nous avons 47 malades qui vivent sans ictère, dont 24 depuis plus de 5 ans. Les plus longues survies atteignent 23 ans. Tous ont une vie normale pour leur âge, malgré le fait que 7 d'entre eux présentaient certains handicaps physiques ou mentaux. Le succès de l'hépaticoentérostomie dépend de la précocité de l'intervention, de la qualité de la technique opératoire et de la prévention de l'angiocholite postopératoire.
Similar content being viewed by others
References
Kasai, M., Watanabe, I., Ohi, R.: Follow-up studies of long-term survivors after hepatic portoenterostomy for “noncorrectable” biliary atresia. J. Pediatr. Surg.10:173, 1975
Miyata, M., Satani, M., Ueda, T., Okamoto, E.: Long-term results of hepatic portoenterostomy for biliary atresia: special reference to postoperative portal hypertension. Surgery76:234, 1974
Kobayashi, A., Utsunomiya, T., Kawai, S., Ohbe, Y.: Congenital biliary atresia: analysis of 97 cases with reference to prognosis after hepatic portoenterostomy. Am. J. Dis. Child.130:830, 1976
Airman, R.P., Chandra, R., Lilly, J.R.: Ongoing cirrhosis after successful porticoenterostomy in infants with biliary atresia. J. Pediatr. Surg.10:685, 1975
Odièvre, M., Valayer, J., Razemon-Pinta, M., Habib, E., Alagille, D.: Hepatic portoenterostomy or cholecystostomy in the treatment of extrahepatic biliary atresia. J. Pediatr.88:774, 1976
Carcassonne, M., Bensoussan, A.: Long-term results in treatment of biliary atresia. Prog. Pediatr. Surg.10:151, 1977
Sawaguchi, S., Akiyama, Y., Saeki, M., Ohta, Y.: The treatment of congenital biliary atresia, with special reference to hepatic portoentero-anastomosis. Fifth Annual Meeting of the Pacific Association of Pediatric Surgeons, 1972, Tokyo, Japan
Kasai, M.: Hepatic portoenterostomy and its modifications for “noncorrectable” biliary atresia. Paediatrician3:204, 1974
Kasai, M.: Treatment of biliary atresia with special reference to hepatic portoenterostomy and its modifications. Prog. Pediatr. Surg.6:5, 1974
Suruga, K., Nagashima, K., Kohno, S., Miyano, T., Kitahara, T., Inui, M.: A clinical and pathological study of congenital biliary atresia. J. Pediatr. Surg.7:655, 1972
Lilly, J.R., Altman, R.P.: Hepatic portoenterostomy (the Kasai operation) for biliary atresia. Surgery78:76, 1975
Ikeda, K., Suita, S.: Hepatic portogastrostomy using a gastric tube for the treatment of congenital biliary atresia. Z. Kinderchir.17:360, 1975
Sterling, J.A.: Artificial bile ducts in the management of congenital biliary atresia: a clinical report. J. Int. Coll. Surg.36:293, 1961
Williams, L.F., Jr., Dolling, J.A.: Thoracic ductesophagus anastomosis for relief of congenital biliary atresia. Surg. Forum14:189, 1963
Suruga, K., Yamazaki, Z., Nagashima, K., Iwai, S., Mori, W.: [A new operation for biliary atresia]. Shuzutsu18:910, 1964
Fonkalsrud, E.W., Kitagawa, S., Longmire, W.P., Jr.: Hepatic lymphatic drainage to the jejunum for congenital biliary atresia. Am. J. Surg.112:188, 1966
Kasai, M., Suzuki, S.: [A new operation for “non-correctable” biliary atresia-hepatic portoenterostomy]. Shuzutsu13:733, 1959
Kasai, M., Kimura, S., Wagatsuma, M., Suzuki, H.: Die chirurgischen Behandlungen der angeborenen Missbildungen des Gallengangs. Therapiewoche12:710, 1963
Kasai, M., Kimura S., Asakura, Y., Suzuki, H., Taira, Y., Ohashi, E.: Surgical treatment of biliary atresia. J. Pediatr. Surg.3:665, 1968
Danks, D.M., Campbell, P.E.: Frequencies of certain liver diseases and abnormalities in Victoria, Australia birth defects. Orig. Article Series8:119, 1972
Ohi, R., Kasai, M., Takahashi, T.: Intrahepatic biliary obstruction in congenital bile duct atresia. Tohoku J. Exp. Med.99:129, 1976
Chiba, T., Kasai, M., Sasano, N.: Reconstruction of intrahepatic bile ducts in congenital biliary atresia. Tohoku J. Exp. Med.115:99, 1975
Chiba, T., Kasai, M., Sasano, N.: Histopathological studies on intrahepatic bile ducts in the vicinity of the porta hepatis in biliary atresia. Tohoku J. Exp. Med.118:199, 1976
Campbell, D.P., Poley, J.R., Bhatia, M., Smith, E.I.: Hepatic portoenterostomy—Is it indicated in the treatment of biliary atresia? J. Pediatr. Surg.9:329, 1974
Altman, R.P.: Portal decompression by interposition mesocaval shunt in patients with biliary atresia. J. Pediatr. Surg.11:809, 1976
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Kasai, M., Suzuki, H., Ohashi, E. et al. Technique and results of operative management of biliary atresia. World J. Surg. 2, 571–579 (1978). https://doi.org/10.1007/BF01556048
Issue Date:
DOI: https://doi.org/10.1007/BF01556048