Results 91 to 100 of about 613,875 (232)

Hepatic Protoenterostomy

open access: yesAnnals of Surgery, 1975
A series of 12 infants undergoing hepatic portoenterostomy for incorrectable-type biliary atresia is reviewed. There has been no evidence of a sustained postoperative increase in bile excretion or improvement in biliary cirrhosis in any patient. Survival statistics for the group as a whole are poor with a mean postop survival time of 11 months and a ...
D P, Campbell   +4 more
openaire   +3 more sources

Liver transplantation for biliary atresia [PDF]

open access: yes, 1984
Orthotopic liver transplantation was performed 15 months to 20 years ago in 126 recipients, all of whom were under 18 years of age. Eighty-six of these pediatric recipients were treated before 1980 with azathioprine (or eyclophosphamide) and prednisone ...
Shaw, BW   +3 more
core   +1 more source

Relation between degrees of hepatic fibrosis and post-operative Jaundice clearance in patients with extra hepatic biliary atresia; observational study

open access: yesMinia Journal of Medical Research
Biliary atresia is a obstructive cholangiopathy and the leading cause of neonatal cholestasis. Kasai portoenterostomy (KPE) is the initial treatment, outcomes vary significantly.
Mahmoud Mohamed   +5 more
doaj   +1 more source

Bile duct matrix metalloproteinase-7 expression: a new modality for diagnosis of biliary atresia

open access: yesEgyptian Liver Journal
Background Biliary atresia (BA) is an obliterative cholangiopathy of infancy that results in cholestasis and liver fibrosis. This fibrosis is due to an imbalance in extracellular matrix (ECM) breakdown and deposition.
Alif Abdelhakim Allam   +4 more
doaj   +1 more source

A histopathological study of liver and biliary remnants in the long-term survivors (>10 years) of cases of biliary atresia

open access: yesIndian Journal of Pathology and Microbiology, 2014
Context: Biliary atresia (BA) is a destructive process affecting both extra- and intra-hepatic bile ducts leading to fibrosis and obliteration of the biliary tree and cirrhosis usually within 2 years.
Sabuj Ghana Mukhopadhyay   +7 more
doaj   +1 more source

Hepatolithiasis after hepatic portoenterostomy for biliary atresia

open access: yes
Background Hepatolithiasis after hepatic portoenterostomy for biliary atresia has been paid little attention, with only 22 reported cases. Patients and Methods Fifteen patients underwent living-related liver transplantation for biliary atresia after ...
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core  

Abstract

open access: yes
JPGN Reports, Volume 6, Issue S2, Page S1-S814, September 2025.
wiley   +1 more source

Common bile duct cysts in neonates, not always a choledochal cyst: A case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Obstructive jaundice in neonates results from disruption of bile drainage from the liver, which may be related to several conditions. Differentiating between these conditions and intervening rapidly is critical, as the success of treatment ...
Josephine Issenman, Kathryn Martin
doaj   +1 more source

PATHOPHYSIOLOGY, CLINICAL FEATURES, AND MANAGEMENT OF CHILDREN WITH CHRONIC INFECTIOUS DISEASES

open access: yes, 2009
Children with chronic diseases Chronic viral hepatitis Among human hepatitis viruses, hepatitis B (HBV) and C (HCV) viruses are able to persist in the host for years and thereby causing chronic hepatitis.
Giannattasio, Antonietta
core  

A study on cholangitis after hepatic portoenterostomy for biliary atresia.

open access: yesChinese medical journal, 1998
To investigate the clinical manifestations and factors relating to prognosis in biliary atresia (BA).Twenty-four cases were reviewed on clinical manifestations and bile flow after operation. All patients underwent hepatic portoenterostomy.Twenty-three cases (95%) got bile flow postoperatively. Sixteen (69%) of 23 patients had 27 episodes of cholangitis.
J, Liu, G, Li, B, Lai
openaire   +1 more source

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