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choledochal cyst/edema

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ArtículosEnsayos clínicosPatentes
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Choledochal cysts are uncommon congenital anomalies of the biliary tree, commonly presenting in infancy, generally in the 1(st) year of life. Presentation in adult life is less common, accounting for 20% of cases. A 19-year-old female patient presented to the Emergency Department with severe

Massive hydrops of the gallbladder mimicking a choledochal cyst.

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Choledochal cyst associated with acute acalculous cholecystitis.

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A 7-year-old girl underwent laparotomy for suspected acute appendicitis. Instead, bile peritonitis with hydrops of gallbladder and normal appendix were noted. Dilatation of the CBD was observed, and choledochal cyst was documented by intraoperative cholangiography. Cholecystectomy and T-tube

[Application of enhanced recovery after surgery in the treatment of children with congenital choledochal cyst].

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To explore the feasibility of enhanced recovery after surgery (ERAS) in treatment of children with congenital choledochal cyst.

METHODS
One hundred and thirty children with congenital choledochal cysts admitted in the Children's Hospital of Zhejiang

Usefulness of laparoscopic cholecystostomy in children with complicated choledochal cyst.

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BACKGROUND In children with choledochal cysts (CC), obstruction of the discharge of bile or pancreatic juice is frequently observed, and biliary perforation and severe pancreatitis may occur. In such cases, temporary drainage is necessary to stabilize these patients. We employed laparoscopic
BACKGROUND This study aimed to present the authors' technique and the intermediate-term outcome for laparoscopic choledochal cyst excision with Roux-en-Y hepatoenterostomy. METHODS This retrospective study investigated 62 children (39 girls and 23 boys) who had undergone laparoscopic resection of

Neuroendocrine tumor of the common hepatic duct, mimicking a choledochal cyst in a 6-year-old child.

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We report a rare case of a neuroendocrine tumor of the extrahepatic biliary tree in a child. A 6-year-old girl who presented with jaundice and pruritus was found to have elevated liver enzymes along with a cystic dilatation of the common hepatic duct. After further diagnostic testing, a working

[Differential sonographic diagnosis. Pancreas (pseudo) cyst--choledochus cyst].

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The case of a woman patient with an extended prepapillary choledochal cyst and pancreaticobiliary reflux shows that it is necessary to consider the possibility of a choledochal cyst on detecting a cystic structure in the head of the pancreas (condition after acute pancreatitis); besides this,

Interposition of the gallbladder--or the absent common hepatic duct and cystic duct.

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Interposition of the gallbladder is a rare anomaly, but its diagnosis is important since it represents a surgically correctable cause of jaundice. The patients present with jaundice, abdominal pain and sometimes an enlarged gallbladder. Radiological diagnosis may be difficult since the condition may
Endoscopic ultrasound (EUS)-assisted biliary access is utilized when conventional endoscopic retrograde cholangiopancreatography (ERCP) fails. We report a 10-year experience utilizing a transduodenal EUS rendezvous via a transpapillary route without dilation of the transduodenal tract, followed by

Giant cystic abdominal masses in children.

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In this pictorial essay the common and uncommon causes of large cystic and cyst-like abdominal masses in children are reviewed. We discuss and illustrate the following: mesenchymal hamartoma, choledochal cyst, hydrops of the gallbladder, congenital splenic cyst, pancreatic pseudocyst, pancreatic
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