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Cystic Biliary Atresia:Why Is It Important to Distinguish this from Congenital Choledochal Cyst?

Authors :
Mohammed Hamdy, Hussein Ahmed
Zaidan, Hind Mustafa
Corbally, Martin
Source :
Bahrain Medical Bulletin. Jun2014, Vol. 36 Issue 2, p105-107. 3p.
Publication Year :
2014

Abstract

We present a 2-month-old jaundiced infant with a rare type of biliary atresia who appeared to have a choledochal cyst on Magnetic Resonance Cholangiopancreatography (MRCP) and ultrasound. Intra-operative findings were the only proof of biliary atresia. Following portoenterostomy, Liver Function Tests (LFTs) and bilirubin levels were returned within normal range and his jaundice was resolved. Any neonate presenting to a pediatric clinic with prolonged jaundice lasting more than two weeks, especially in cases of direct hyperbilirubinemia, must be thoroughly assessed and referred as early as possible for a pediatric surgical opinion to rule out the possibility of biliary atresia. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10128298
Volume :
36
Issue :
2
Database :
Academic Search Index
Journal :
Bahrain Medical Bulletin
Publication Type :
Academic Journal
Accession number :
96452610
Full Text :
https://doi.org/10.12816/0004489