Results 41 to 50 of about 80,892 (209)
Journal of Genetic Counseling, Volume 35, Issue 6, December 2026.ABSTRACT Germline genetic testing in the pediatric oncology population remains under‐utilized, despite evidence that 10%–15% of these patients have an underlying genetic cause. Identifying patients with a genetic predisposition can affect diagnosis, treatment, and future surveillance of the patient and family.
Camille Hamilton +14 more
wiley +1 more source
The Surgery Journal, 2022 Introduction Choledochal cyst is a premalignant condition and surgical excision with biliary enteric anastomosis is the standard of care. Surgical treatment in adults may be difficult due to associated biliary pathology and high incidence of ...
Aravinth Anbarasu, Aparna Deshpande
doaj +1 more source
Advanced Science, Volume 13, Issue 50, 7 September 2026.Expanded NCAM1+EpCAM+ hepatic progenitor cells in biliary atresia are characterized by aggregation of α‐synuclein. This pathological protein potentiates cellular susceptibility to GSH‐dependent redox dyshomeostasis, induces unstable biliary cell fate specification, and subsequently drives aberrant biliary regeneration.
Hua Xie +12 more
wiley +1 more source
Children, 2020 The concomitant occurrence of duodenal atresia (DA) and a choledochal cyst (CC) has rarely been reported. Knowledge of both the presentation and management of this rare co-occurrence is imperative in avoiding potential complications and sequelae, such as
Brittany Downing +3 more
doaj +1 more source
Percutaneous transhepatic electrohydraulic lithotripsy for intrahepatic bile duct stones after choledochal cyst excision [PDF]
, 2012 Excision and hepaticojejunostomy are well-established treatments for choledochal cysts. However, the formation of intrahepatic bile duct stones has been reported as one of the most serious long-term complications on follow-up of choledochal cyst excision.
Nagayasu, Takeshi +4 more
core
United European Gastroenterology Journal, Volume 14, Issue 7, September 2026.ABSTRACT Background Aggressive peri‐procedural intravenous fluid (IVF) therapy with lactated Ringer's solution (LR) reduces the risk of post‐ERCP pancreatitis (PEP), but the standard 8‐h protocol is impractical in outpatient settings and the optimal fluid type remains uncertain.
Woo Hyun Paik +20 more
wiley +1 more source
American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Journal of British Surgery, 1974 Abstract This paper reports a series of 8 children with a choledochal cyst. The pathology, diagnosis and treatment of choledochal cyst are discussed. All the cases have been fully followed up and 1 patient has been examined 21 years after operation.
openaire +2 more sources
Pseudopancreatitis and choledochal cyst [PDF]
Revista Española de Enfermedades Digestivas, 2004 choledocal cysts (1). Although it is considered a congenital illness, 30% of cases are diagnosed in the adult age. Clinical symptoms are quite variable: the classical triad of abdominal pain, jaundice and abdominal mass is exceptional in adult subjects.
Pareja Ibars,E. +5 more
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Journal of Gastroenterology and Hepatology, Volume 41, Issue 6, Page 1701-1721, June 2026.ABSTRACT Intrahepatic cholangiocarcinoma (iCCA) ranks as the second most common primary liver cancer, compared to about 20% of cases. Its global incidence has climbed over the past four decades, yet early detection remains indefinable due to its asymptomatic nature. Five‐year survival rate of approximately is under 10%.
Yaqoob Muhammad +10 more
wiley +1 more source