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References
Balistreri WF, Grand R, Hoofnagle JH, et al (1996) Biliary atresia: current concepts and research directions. Hepatology 23: 1682–92
Caroli J, Couilhaud C (1958) Une affection nouvelle, sans doute congenitale, des voies biliaires: la dilatation kystique unilobaire eds canaux hepatiques. Sem Hosp Paris 14: 496–502
Caroli J, Corcos V (1964) Maladies des voies biliaires intrahépatiques segmentaires. Masson et Cie, Paris, pp 59–154
DeRusso PA, Ye W, Shepherd R, et al (2007) Growth failure and outcomes in infants with biliary atresia: a report from the Biliary Atresia Research Consortium. Hepatology 46: 1632–8
Desmet VJ (1992) Congenital diseases of intrahepatic bile ducts: variations on the theme “Ductal plate malformation”. Hepatology 16: 1069–83
Desmet VJ, Eyken P (1995) Embryology, malformations, and malpositions of the liver. In: Haubrich WS, Schaffner F (eds) Bockus gastroenterology, 5th edn. W.B. Saunders, Philadelphia, PA, pp 1849–57
Fozard JB, Wyatt JI, Hall RI (1989) Epithelial dysplasia in Caroli's disease. Gut 30: 1150–3
Giovanardi RO (2003) Monolobar Caroli's disease in an adult. Case report. Hepatogastroenterology 50: 2185–7
Kasai M, Kimura S, Asakura S, et al (1968) Surgical treatment of biliary atresia. J Pediatr Surg 3: 665–75
Kirchner GI, Wagner S, Flemming P, et al (2002) COACH syndrome associated with multifocal liver tumors. Am J Gastroenterol 97: 2664–9
Lykavieris P, Chardot C, Sokhn M, et al (2005) Outcome in adulthood of biliary atresia: a study of 63 patients who survived for over 20 years with their native liver. Hepatology 41: 366–71
Mack CL, Tucker RM, Lu BR, et al (2006) Cellular and humoral autoimmunity directed at bile duct epithelia in murine biliary atresia. Hepatology 44: 1231–9
Mindikoglu AL, Regev A, O'Sullivan MJ, et al (2005) Multiple normal deliveries in a woman with severe portal hypertension due to congenital hepatic fibrosis: the importance of preserved hepatocellular function. Am J Gastro enterol 100: 2359–61
Mowat AP (1996) Biliary atresia into the 21st century: a historical perspective. Hepatology 23: 1693–5
Muise AM, Turner D, Wine E, et al (2006) Biliary atresia with choledochal cyst: implications for classification. Clin Gastroenterol Hepatol 4: 1411–4
Narayanaswamy B, Gonde C, Tredger JM, et al (2007) Serial circulating markers of inflammation in biliary atresia – evolution of the post-operative inflammatory process. Hepatology 46: 180–7
Remmele W (1984) Gallenblase, extrahepatische Gal lengänge, Vatersche Papille. In: Remmele W (Hrsg), Pathologie, Bd. 2. Ein Lehr- und Nachschlagebuch. Springer Verlag, Berlin, Heidelberg, New York pp 741–88
Ros E, Navarro S, Bru C, et al. (1993) Ursodeoxycholic acid treatment of primary hepatolithiasis in Caroli's syndrome. Lancet 342: 404–6
Saito T, Shinozaki K, Matsunaga T, et al (2004) Lack of evidence for reovirus infection in tissues from patients with biliary atresia and congenital dilatation of the bile duct. J Hepatol 40: 203–11
Taylor ACF, Palmer KR (1998) Caroli's disease. Euro J Gastroenterol Hepatol 10: 105–8
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Dancygier, H. (2010). Bile Duct Anomalies. In: Clinical Hepatology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-04519-6_2
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