Results 81 to 90 of about 7,207 (227)

Bile Duct Replacement in Hepatobiliary Surgery: A Systematic Review

open access: yesWorld Journal of Surgery, Volume 49, Issue 11, Page 3182-3194, November 2025.
Roux‐en‐Y hepaticojejunostomy (RYHJ) is currently the standard surgical technique for reestablishing biliary continuity, but it exposes the patient to serious biliary complications, such as anastomosis stricture and ascending cholangitis. RYHJ also limits access to the biliary tree for endoscopic intervention in cases with biliary complications, making
Mehdi Boubaddi   +9 more
wiley   +1 more source

Prenatal diagnosis of a giant choledochal cyst

open access: yesJournal of Pediatric Surgery Case Reports, 2016
A choledochal cyst is a rare and usually benign condition that is diagnosed in 80% of cases in early infancy. Prenatal diagnosis is increasingly identifying the cysts allowing an early surgical treatment with less risk of complications.
Yurema González Ruiz   +6 more
doaj   +1 more source

Assessment of Donor‐Specific Human Leukocyte Antigen Antibodies Following Pediatric Liver Transplantation: Predictors, Protectors, and Clinical Relevance

open access: yesClinical Transplantation, Volume 39, Issue 11, November 2025.
ABSTRACT Background Following pediatric liver transplantation (pLT), the significance and management of donor‐specific antibodies (DSA) against human leukocyte antigen (HLA) remain undefined. The aim of this single‐center study was to investigate the occurrence of DSA, their clinical impact on predictors for and protectors against DSA.
Evelien Kanaan   +9 more
wiley   +1 more source

Diverticular Choledochal Cyst with a Large Impacted Stone Masquerading as Mirizzi's Syndrome

open access: yesCase Reports in Gastroenterology, 2013
Choledochal cysts are congenital anomalies of the biliary tract manifested by cystic dilatation of the extrahepatic and intrahepatic bile ducts. Choledochal cyst is not rare in far-East Asian countries.
Soon Oh Hwang   +7 more
doaj   +1 more source

A prediction model for genetic cholestatic disease in infancy using the machine learning approach

open access: yesJournal of Pediatric Gastroenterology and Nutrition, Volume 81, Issue 4, Page 933-942, October 2025.
Diagnostic algorithm for cholestatic infants. Abstract Objectives Cholestasis in infancy poses a complex clinical conundrum for pediatric hepatologists, warranting timely diagnosis, especially for genetic diseases. This study aims to create machine learning (ML)‐based prediction models, referred to as Jaundice Diagnosis Easy for Baby (JADE‐B), to ...
Chi‐San Tai   +9 more
wiley   +1 more source

Right hemihepatectomy for bile duct injury following laparoscopic cholecystectomy [PDF]

open access: yes, 2018
Laparoscopic cholecystectomy (LC) has become the treatment of choice for patients with symptomatic cholecystolithiasis. But with the introduction of this technique, the incidence of bile duct injuries has increased.
Fellbaum, C.   +4 more
core  

Endoscopic Unroofing of a Choledochocele [PDF]

open access: yes, 2017
A 42-year-old man with previous laparoscopic cholecystectomy was referred for further evaluation of recurrent acute pancreatitis. Secretin-enhanced magnetic resonance cholangiopancreatography showed a 16 mm × 11 mm T2 hyperintense cystic lesion at the ...
El Hajj, Ihab I.   +3 more
core   +1 more source

Giant Choledochal Cyst in an Adult at a Teaching Hospital in South-Western Uganda: A Case Report

open access: yesInternational Medical Case Reports Journal, 2021
Mvuyo Maqhawe Sikhondze,1 Carlos Cabrera Dreque,1 Edson Tayebwa,1 Gotharido Tumubugane,1 Charles Newton Odongo,1 Eugene Ogwang2 1Department of Surgery, Mbarara University of Science and Technology, Mbarara City, South-Western Uganda, Uganda; 2Department ...
Sikhondze MM   +5 more
doaj  

Simpson-Golabi-Behmel syndrome types I and II [PDF]

open access: yes, 2014
Simpson-Golabi-Behmel syndrome (SGBS) is a rare overgrowth syndrome clinically characterized by multiple congenital abnormalities, pre/postnatal overgrowth, distinctive craniofacial features, macrocephaly, and organomegaly.
Fernando Santos   +6 more
core   +1 more source

A Choledochal Cyst Resulting in Obstructive Jaundice in a Case with Gallbladder Agenesis: Report of a Case and Review of the Literature

open access: yesBalkan Medical Journal, 2012
Co-existence of gallbladder agenesis and choledochal cyst is a very rare congenital anomaly of the extrahepatic biliary system. The literature presents only five cases with this combination. Herein, we report the sixth case.
Abdullah Böyük   +4 more
doaj  

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