Biliary atresia type I cyst and choledochal cust: can we differentiate or not?

SUZUKI Tatsuya; HASHIMOTO Takashi; HUSSEIN Mohamed Hamed; HARA Fujio; HIBI Masahito; KATO Takazumi

Art

J-GLOBAL ID：201302237773437844 Reference number：13A1123052

Biliary atresia type I cyst and choledochal cust: can we differentiate or not?

I cyst型胆道閉鎖症と総胆管嚢胞:鑑別可能か,それとも不可能か?

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Material：
Volume： 20 Issue： 5 Page： 465-471 Publication year： Jun. 2013
JST Material Number： L4083A ISSN： 1868-6974 Document type： Article
Article type：原著論文 Country of issue： Japan (JPN) Language： ENGLISH (EN)

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Digestive system diagnosis , Diagnostics of congenital diseases, deformities.

Reference (27)：

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KASAI, M. A proposal of new classification of biliary atresia. J Jpn Soc Pediatr Surg. 1976, 12, 327-331
RUIZ-ELIZALDE, AR. A practical algorithm for accurate diagnosis and treatment of perinatally identified biliary ductal dilation : three cases that underscore the importance of an individualised approach. J Matern Fetal Neonatal Med. 2009, 22, 622-628
OKADA, T. Postnatal management for prenatally diagnosed choledochal cysts. J Pediatr Surg. 2004, 39, 1055-1058
ZHOU, LY. Objective differential characteristics of cystic biliary atresia and choledochal cysts in neonates and young infants : sonographic findings. J Ultrasound Med. 2012, 31, 833-841

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