Results 61 to 70 of about 456,499 (267)
Type IVA choledochal cyst: a rare cause of cirrhosis in adults
The Egyptian Journal of Internal Medicine, 2022 Background Choledochal cysts (CDCs) are characterized by congenital cystic dilations of the intrahepatic or extrahepatic bile ducts or both. CDCs are very rarely reported in sub-Saharan Africa.
Chantelli Iamblaudiot Razafindrazoto +9 more
doaj +1 more source
Ultrasound in Obstetrics &Gynecology, EarlyView.ABSTRACT Objective The primary aim was to evaluate pre‐ and postnatal morphological changes in large simple fetal ovarian cysts following in‐utero aspiration compared with expectant management. Secondary aims were to assess postnatal outcome in terms of surgical intervention and to evaluate complications associated with in‐utero aspiration.
V. Peyronnet +10 more
wiley +1 more source
Congenital choledochal cyst in an infant with cystic fibrosis
Annals of Hepatology, 2009 Congenital choledochal cyst is malformation of the biliary ductal system, which rarely occur. We describe here a 4-month old boy, who was referred to our center with respiratory distress and low level consciousness.
Parviz Tabatabaie +7 more
doaj +1 more source
Child with Choledochal Cyst Presenting with Episodes of Vomitting and Jaundice [PDF]
, 2009 A 2 year old girl presented to the emergency department with frequent episodes of vomiting and jaundice. Analytically, there was leucocytosis with normal neutrophil count, RCP of 5, 66 mg/dL and GGT 87 U/L.
Almeida, J +5 more
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Acta Paediatrica, EarlyView.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
A 10-year-old Boy with Giant Choledochal Cyst: A Case Report
Archives of Pediatric Gastroenterology, Hepatology, and Nutrition, 2022 Choledochal duct cyst is a rare congenital anomaly in the form of cystic dilatation of both intrahepatic and extrahepatic bile ducts. The clinical symptoms of choledochal cysts are generally due to bile stasis, stone formation, recurrent superinfection,
Ninung RD Kusumawati, Juwita Pratiwi
doaj +1 more source
Bile Duct Replacement in Hepatobiliary Surgery: A Systematic Review
World 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
Type I Choledochal Cyst Complicated With Acute Hemorrhagic Pancreatitis: A Case Report
Journal of Medical Ultrasound, 2017 Choledochal cysts rarely present with acute pancreatitis. We report a patient with type I choledochal cyst(s) who had concomitant acute frank hemorrhagic pancreatitis.
Ping-Hua Tsai +10 more
doaj +1 more source
A prediction model for genetic cholestatic disease in infancy using the machine learning approach
Journal 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
Biliary atresia associated with choledochal cyst
African Journal of Paediatric Surgery, 2009 Choledochal cyst and biliary atresia are rare but important causes of neonatal jaundice. Both present with jaundice and acholic stool in neonatal period. Treatment and prognosis of both entities are very different.
Obaidah Abu +3 more
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