Results 51 to 60 of about 457,270 (221)
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
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
Pancreatic fistula and bleeding following choledochal cyst excision: Experience of two decades. [PDF]
Turk J SurgKrishna Katakam S +8 more
europepmc +2 more sources
Ultrasound in Obstetrics &Gynecology, Volume 67, Issue 1, Page 60-66, January 2026.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
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
Acta Paediatrica, Volume 115, Issue 1, Page 196-201, January 2026.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
Early complications after laparoscopic resection of choledochal cyst
Pediatric surgery international (Print), 2019 PurposeTo investigate the causes and treatments of early complications involving laparoscopic radical resection of choledochal cyst and summarize the experience.MethodsChildren with choledochal cyst treated by laparoscopy in the Department of Pediatric ...
Bing Zhang +7 more
semanticscholar +1 more source
Asian Journal of Endoscopic Surgery, Volume 19, Issue 1, January/December 2026.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
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
doaj
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