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Acta Chirurgica Belgica, 1998
A case of choledochal cyst in an adult is presented. Preoperative diagnosis was established by CT-scanning and MRI. The patient was treated with cyst excision and Roux-en-Y hepaticojejunostomy. A review of the literature is presented.
M. R. P. Van den Bossche, R. Vercruysse
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A case of choledochal cyst in an adult is presented. Preoperative diagnosis was established by CT-scanning and MRI. The patient was treated with cyst excision and Roux-en-Y hepaticojejunostomy. A review of the literature is presented.
M. R. P. Van den Bossche, R. Vercruysse
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Fetal and Pediatric Pathology, 2019
Introduction: Both cystic biliary atresia and choledochal cyst present as infantile obstructive cholangiopathy. Methods: We detail an infant with congenital biliary dilatation and obstructive cholangiopathy where clinicoradiological features (antenatally
S. Mahalik, S. Mitra, S. Patra, K. Das
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Introduction: Both cystic biliary atresia and choledochal cyst present as infantile obstructive cholangiopathy. Methods: We detail an infant with congenital biliary dilatation and obstructive cholangiopathy where clinicoradiological features (antenatally
S. Mahalik, S. Mitra, S. Patra, K. Das
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Periampullary choledochal diverticula are not choledochal cysts
Gastrointestinal Endoscopy, 2011Choledochal cysts (CC) are rare, congenital anomalies of the biliary tree, associated with the development of biliary malignancies. Small periampullary choledochal diverticula (PCD) are a previously unreported type of biliary anomaly found primarily at ERCP.The aim of this study was to assess whether PCD are congenital or acquired lesions by comparing ...
Glen A. Lehman +6 more
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Abdominal Imaging, 2015
Choledochal cysts are rare cystic dilatations of the intrahepatic and/or extrahepatic biliary tree, which may be mistaken for other cystic lesions if their characteristic features are not recognized. The etiology is unknown, and likely multifactorial, and it is uncertain whether they are congenital or acquired.
Vahid Yaghmai +6 more
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Choledochal cysts are rare cystic dilatations of the intrahepatic and/or extrahepatic biliary tree, which may be mistaken for other cystic lesions if their characteristic features are not recognized. The etiology is unknown, and likely multifactorial, and it is uncertain whether they are congenital or acquired.
Vahid Yaghmai +6 more
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Choledochoceles: Are They Choledochal Cysts?
Advances in Surgery, 2011The classification of choledochoceles as a type of choledochal cyst stems from the 1959 article by Alonso-Lej and colleagues describing 94 choledochal cysts, only 4 of which were choledochoceles. Even then, Alonso-Lej questioned the propriety of including the choledochocele, stating it was unclear "as to whether or not it originates from the same ...
Nicholas J. Zyromski, Kathryn M. Ziegler
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Journal of Gastroenterology and Hepatology, 1997
ABSTRACTWe report a case of Caroli's disease associated with diverticulae and choledochocele of the common bile duct, a wide pancreaticobiliary angle and non‐cirrhotic portal hypertension. This patient presented with recurrent episodes of cholangitis. To our knowledge, such a range of findings in the same patient has not been previously reported in the
Vivek A. Saraswat +3 more
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ABSTRACTWe report a case of Caroli's disease associated with diverticulae and choledochocele of the common bile duct, a wide pancreaticobiliary angle and non‐cirrhotic portal hypertension. This patient presented with recurrent episodes of cholangitis. To our knowledge, such a range of findings in the same patient has not been previously reported in the
Vivek A. Saraswat +3 more
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JAMA: The Journal of the American Medical Association, 1967
Choledochal cysts are congenital malformations and can be classified into four types. The type 1 lesion is the usual form; the others are extremely uncommon. The treatment in most cases should be surgical drainage into the gastrointestinal tract, preferably using the jejunum in Roux-en-Y fashion.
J R Macfarlane, F Glenn
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Choledochal cysts are congenital malformations and can be classified into four types. The type 1 lesion is the usual form; the others are extremely uncommon. The treatment in most cases should be surgical drainage into the gastrointestinal tract, preferably using the jejunum in Roux-en-Y fashion.
J R Macfarlane, F Glenn
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Management of choledochal cysts
Current Opinion in Gastroenterology, 2016Historically, surgical treatment of choledochal cyst consisted of cyst enterostomy. However, incomplete cyst excision can result in recurrent symptoms and malignant transformation within the cyst remnant. Accordingly, management of choledochal cyst now includes complete cyst excision whenever possible.
Aslam Ejaz +3 more
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Pediatric surgery international (Print), 2021
D. Hinojosa-González +4 more
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D. Hinojosa-González +4 more
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Archives of Surgery, 1976
Cystic dilation of the common bile duct is a rare congenital anomaly. The cases of two patients, 2 1/2 and 18 years old, respectively, illustrate the difficulty in preoperative diagnosis, as well as the value of long-term postoperative follow-up. Ascending cholangitis developed in one of the patients after a Roux-en-Y cystojejunostomy nine years after ...
Sami Obeid +2 more
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Cystic dilation of the common bile duct is a rare congenital anomaly. The cases of two patients, 2 1/2 and 18 years old, respectively, illustrate the difficulty in preoperative diagnosis, as well as the value of long-term postoperative follow-up. Ascending cholangitis developed in one of the patients after a Roux-en-Y cystojejunostomy nine years after ...
Sami Obeid +2 more
openaire +3 more sources