Cystic Biliary Atresia: Confounding and Intriguing

2012 ◽  
Vol 161 (3) ◽  
pp. 562 ◽  
Author(s):  
Ankur Arora ◽  
Yashwant Patidar ◽  
Rajeev Khanna ◽  
Seema Alam ◽  
Archana Rastogi ◽  
...  
2021 ◽  
Vol 66 ◽  
pp. 101781
Author(s):  
C.L. Berkowitz ◽  
A.W. Peters ◽  
J.D. Stratigis ◽  
P.D. Barone ◽  
A.V. Kadenhe-Chiweshe ◽  
...  

2017 ◽  
Vol 41 (3) ◽  
pp. 354-364 ◽  
Author(s):  
Inna N. Lobeck ◽  
Rachel Sheridan ◽  
Mark Lovell ◽  
Phylicia Dupree ◽  
Greg M. Tiao ◽  
...  

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

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

2005 ◽  
Vol 8 (6) ◽  
pp. 725-731 ◽  
Author(s):  
Vera De Matos ◽  
Jessi Erlichman ◽  
Pierre A. Russo ◽  
Barbara A. Haber

We describe a unique series of 3 cases of biliary atresia (BA) associated with a choledochal cyst. All 3 children presented with jaundice at birth and had no other abnormalities. Although these children had a fetal form of BA, their presentation and outcome differed from those of biliary atresia splenic malformation syndrome (BASM), the well-described form of early onset BA. Unlike those with BASM, these children had no other associated malformations, had a normal birth weight, and did not yet require a liver transplant. We believe that the present series of patients and their associated pathology may represent a distinct phenotype with a common, prenatally acquired etiology that is different from other fetal forms of BA, such as BASM, and from patients who present with the classic perinatal form of BA.


2017 ◽  
Vol 54 (4) ◽  
pp. 383-389
Author(s):  
Jue Tang ◽  
Dan Zhang ◽  
Wei Liu ◽  
Ji-Xiao Zeng ◽  
Jia-Kang Yu ◽  
...  

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