Results 71 to 80 of about 80,892 (209)
Diverticular Choledochal Cyst with a Large Impacted Stone Masquerading as Mirizzi's Syndrome
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
ABSTRACT Aim Solitary functioning kidney (SFK) is linked to chronic kidney disease (CKD) in children, particularly when associated with congenital anomalies of the kidney and urinary tract (CAKUT). Pelvi‐ureteric junction obstruction (PUJO) is the most frequent obstructive uropathy in SFK.
Mathilde Grapin +9 more
wiley +1 more source
ABSTRACT Introduction With the aim of facilitating cross‐specialty discussion on detailed anatomical interpretations in congenital biliary dilatation surgery, the Japan Society for Endoscopic Surgery (JSES) and the Consensus Meeting of Anatomy on the Border (AOB) developed a series of consensus statements in 2024.
Masahiro Takeda +20 more
wiley +1 more source
Primary Epidermoid Cyst of Biliary Duct Presenting as Choledochal Cyst
© SAGE Publications. Choledochal cyst is a cystic dilation of the biliary tree that can increase the risk of malignancy in bile ducts and the gallbladder.
Kwon, Dong Hyang +5 more
core +1 more source
In a national cohort of 3,501 pediatric liver transplants, waitlist access and mortality were similar across racial groups, but survival diverged after transplantation. Non‐Hispanic Black children had a 53% higher risk of post‐transplant mortality (aHR 1.53) and lower 1‐year survival (94.8% vs 96.8%) compared with non‐Hispanic White recipients.
Ahmad Anouti +7 more
wiley +1 more source
Akut batın ön tanısıyla acilen ameliyata alınan bir vakada gözlenen koledok kisti takdim edildi. Vakada kistektomiden sonra koledokoduodenostomi ve pankreatik duodenestomi yapıldı.One case of choledochal cyst observed in emergency operation was reported.
core
American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 761-763, March 2026.
Hiromi Sumitomo +3 more
wiley +1 more source
Association of gastroschisis and choledochal cyst
Two infants are described who presented in the neonatal period with a direct hyperbilirubinemia. This was initially presumed to be because of the diagnosis of gastroschisis and the prolonged use of parenteral nutrition.
Serber, Julia +3 more
core
Choledochal cyst: diagnosis in neonates.
We have described the radionuclide scintigraphic and sonographic findings in two cases of neonatal choledochal cyst.
Hurst, R W +3 more
core +1 more source
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

