Results 71 to 80 of about 31,874 (263)

Simultaneous pancreaticoduodenectomy and liver transplantation for biliary atresia complicated by choledochal cyst

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Children with biliary atresia (BA), a progressive, fibro-obliterative disorder of the intrahepatic and extrahepatic bile ducts in neonates will eventually develop decompensated cirrhotic liver and require liver transplantation (LT).
Yi Luo   +5 more
doaj   +1 more source

Multiple cholangiocarcinomas in the intrahepatic and extrahepatic biliary tree due to dichloromethane exposure: a case report

open access: yesSurgical Case Reports, 2020
Background An outbreak of cholangiocarcinoma in Japan has led to widespread concern among workers in printing plants. In March 2013, the Japanese Ministry of Health, Labour and Welfare, confirmed a causal relationship between cholangiocarcinoma and long ...
Daisuke Ogawa   +9 more
doaj   +1 more source

CONGENITAL MALFORMATION OF THE LIVER IN A NEWBORN (CLINICAL CASE)

open access: yesМать и дитя в Кузбассе, 2020
Congenital hyperplasia of the intrahepatic bile ducts refers to early fetopathy. It represents a «bizarre» proliferation of bile ducts in the portal tract with excessive development of connective tissue.
Наталья Анатольевна Батина   +6 more
doaj  

Emergencies in neonatal management: jaundice and biliary atresia [PDF]

open access: yes, 2016
Biliary atresia is a severe and progressive inflammatory process of unknown cause, which initially involves the extrahepatic bile ducts but which quickly proceeds towards the intrahepatic bile tree leading rapidly to biliary cirrhosis. Biliary atresia is
Clemente, Maria Grazia   +1 more
core  

Cholangiographic findings in hepatic artery occlusion after liver transplantation [PDF]

open access: yes, 1987
Because the hepatic artery provides the only blood supply to the biliary tree of a liver allograft, posttransplantation arterial occlusion may result in a biliary complication.
Bron, KM   +6 more
core   +1 more source

A case report of vanishing bile duct syndrome after exposure to pexidartinib (PLX3397) and paclitaxel. [PDF]

open access: yes, 2019
Pexidartinib (PLX3397) is a small molecule tyrosine kinase and colony-stimulating factor-1 inhibitor with FDA breakthrough therapy designation for tenosynovial giant-cell tumor, and currently under study in several other tumor types, including breast ...
Chien, A Jo   +5 more
core  

Liver transplantation for arteriohepatic dysplasia (Alagille's syndrome) [PDF]

open access: yes, 1992
Thirteen out of 268 children (
Borland, L   +9 more
core   +1 more source

Liver Transplantation for Alagille's Syndrome [PDF]

open access: yes, 1993
Twenty-three children with Alagille's syndrome and end-stage liver disease underwent liver transplantation with cyclosporine and low-dose steroid immunosuppression. Two to 9 years (mean, 4.4 years) after surgery, 13 (57%) of the children were still alive,
Reyes, J   +5 more
core   +1 more source

Alagille syndrome with unusual common bile duct hypoplasia and gallbladder dysmorphism: Lesson based on a case report

open access: yesRadiology Case Reports
Alagille syndrome is an autosomal dominant and multisystemic disease that generally manifests itself with intrahepatic bile ducts paucity, chronic cholestasis, xanthomas and with other less frequent clinical manifestations such as congenital heart ...
Renato Farina, MD   +11 more
doaj   +1 more source

Isolation and primary cultures of human intrahepatic bile ductular epithelium [PDF]

open access: yes, 1988
A technique for the isolation of human intrahepatic bile ductular epithelium, and the establishment of primary cultures using a serum- and growth-factor-supplemented medium combined with a connective tissue substrata is described.
A. E. Sirica   +24 more
core   +1 more source

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