Biliary atresia type I cyst and choledochal cust: can we differentiate or not?
Author:
Affiliation:
1. Department of Pediatric Surgery; Fujita Health University School of Medicine; 1-98 Dengakugakubo, Kutsukake-cho Toyoake Aichi 4701192 Japan
2. Nagoya Nishi Hospital; Nagoya Japan
Publisher
Wiley
Subject
Hepatology,Surgery
Link
http://link.springer.com/content/pdf/10.1007/s00534-013-0605-3
Reference27 articles.
1. Biliary disease in children;Goldman;Curr Gastroenterol Rep.,2011
2. A proposal of new classification of biliary atresia (in Japanese with English abstract);Kasai;J Jpn Soc Pediatr Surg.,1976
3. A practical algorithm for accurate diagnosis and treatment of perinatally identified biliary ductal dilation: three cases that underscore the importance of an individualised approach;Ruiz-Elizalde;J Matern Fetal Neonatal Med.,2009
4. Postnatal management for prenatally diagnosed choledochal cysts;Okada;J Pediatr Surg.,2004
5. Objective differential characteristics of cystic biliary atresia and choledochal cysts in neonates and young infants: sonographic findings;Zhou;J Ultrasound Med.,2012
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1. Vanishing prenatal sub-hepatic cyst associated with biliary atresia: A case report;Journal of Pediatric Surgery Case Reports;2023-09
2. Prenatally diagnosed biliary cysts: A spectrum from congenital biliary dilatation to biliary atresia from the same origin;Journal of Hepato-Biliary-Pancreatic Sciences;2022-05-03
3. Current Understanding in the Clinical Characteristics and Molecular Mechanisms in Different Subtypes of Biliary Atresia;International Journal of Molecular Sciences;2022-04-27
4. Overview of Biliary Atresia;Journal of the Korean Society of Radiology;2022
5. Key imaging features for differentiating cystic biliary atresia from choledochal cyst: prenatal ultrasonography and postnatal ultrasonography and MRI;Ultrasonography;2021-04-01
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