Biliary Atresia: Biliary‐Enteric Drainage or Primary Liver Transplant?

Hepatology ◽  
2019 ◽  
Vol 71 (2) ◽  
pp. 751-752
Author(s):  
Heung Bae Kim ◽  
Scott A. Elisofon

JAMA Surgery ◽  
2019 ◽  
Vol 154 (1) ◽  
pp. 26 ◽  
Author(s):  
Elyse LeeVan ◽  
Lea Matsuoka ◽  
Shu Cao ◽  
Susan Groshen ◽  
Sophoclis Alexopoulos




2018 ◽  
Vol 8 (2) ◽  
pp. 163-166 ◽  
Author(s):  
Ezgi Yangín-Ergon ◽  
Nebahat Ermis ◽  
Ruya Colak ◽  
Burak Polat ◽  
Senem Alkan-Ozdemir ◽  
...  


2015 ◽  
Vol 50 (12) ◽  
pp. 2134-2136 ◽  
Author(s):  
Patrick Ho Yu Chung ◽  
Kenneth Kak Yuen Wong ◽  
See Ching Chan ◽  
Paul Kwong Hang Tam


2018 ◽  
Vol 66 (2) ◽  
pp. 212-217 ◽  
Author(s):  
Danielle Wendel ◽  
Melissa Mortensen ◽  
Alisha Harmeson ◽  
Michele L. Shaffer ◽  
Evelyn Hsu ◽  
...  


2017 ◽  
Vol 60 (2) ◽  
pp. 183-190 ◽  
Author(s):  
Ryota Kikuchi ◽  
Koichi Mizuta ◽  
Taizen Urahashi ◽  
Yukihiro Sanada ◽  
Naoya Yamada ◽  
...  




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.



2010 ◽  
Vol 35 (2) ◽  
pp. 199-202 ◽  
Author(s):  
Suzana Sommer ◽  
Karine Magagnin ◽  
Paulo Kramer ◽  
Maximiano Tovo ◽  
Juliane Bervian

Green pigmentation in teeth is an uncommon condition associated with bilirubin deposits in dental hard tissues. Its occurrence causes anxiety to both child and family. The purpose of this paper is to present a case involving an eleven-year-old girl with green pigmentation of permanent teeth who underwent a liver transplant due to biliary atresia when she was one year old. The reported case confirms the relevance of past medical history in establishing the diagnosis and treatment plan of green teeth.



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