Biliary Atresia, Biliary Hypoplasia, and Choledochal Cyst

Author(s):  
Stephen P. Dunn
2021 ◽  
Vol 66 ◽  
pp. 101781
Author(s):  
C.L. Berkowitz ◽  
A.W. Peters ◽  
J.D. Stratigis ◽  
P.D. Barone ◽  
A.V. Kadenhe-Chiweshe ◽  
...  

2021 ◽  
Vol 68 ◽  
pp. 101837
Author(s):  
Yi Luo ◽  
Dong Zhao ◽  
Tao Zhou ◽  
Jianjun Zhu ◽  
Jianjun Zhang ◽  
...  

2001 ◽  
Vol 26 (6) ◽  
pp. 555-556 ◽  
Author(s):  
STEPHANIE E. SPOTTSWOOD ◽  
PAUL R. JOLLES ◽  
JEFFREY H. HAYNES ◽  
CHARLES E. BAGWELL

2019 ◽  
Vol 38 (6) ◽  
pp. 477-483 ◽  
Author(s):  
Santosh Kumar Mahalik ◽  
Suvradeep Mitra ◽  
Susama Patra ◽  
Kanishka Das

PEDIATRICS ◽  
1978 ◽  
Vol 62 (2) ◽  
pp. 235-237
Author(s):  
Vivian J. Harris ◽  
John Kahler

Obstructive jaundice in young infants represents a clinical situation whose diagnostic evaluation has changed dramatically over the past few years.1-3 Biliary atresia and some forms of neonatal hepatitis are the most common diseases to be differentiated. Emphasis has shifted in recent years toward early surgical exploration for the possibility of performing some form of portoenterostomy. Among surgically correctible lesions, the choledochal cyst, although a rare cause of obstructive jaundice during the newborn period, should be considered and actively pursued since irreversible cirrhosis is a major sequela in untreated cases.4 We describe a patient who was considered to have biliary atresia but on whom a choledochal cyst was discovered at 5½ months of age.


2014 ◽  
Vol 36 (2) ◽  
pp. 105-107
Author(s):  
Hussein Ahmed Mohammed Hamdy ◽  
Hind Mustafa Zaidan ◽  
Martin Corbally

2005 ◽  
Vol 14 (4) ◽  
pp. 206-215 ◽  
Author(s):  
Marcelo Martinez-Ferro ◽  
Edward Esteves ◽  
Pablo Laje

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