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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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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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Transition of Techniques to Treat Choledochal Cysts in Children.
Journal of laparoendoscopic & advanced surgical techniques. Part A, 2016INTRODUCTION Traditionally open resection with hepaticojejunostomy (HJ) reconstruction has been the surgical treatment for cases of choledochal cyst. Our center has recently transitioned from open to laparoscopic and HJ to hepaticoduodenostomy (HD) as ...
Brian G. A. Dalton +4 more
semanticscholar +1 more source
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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Diagnosis and management of choledochal cysts.
HPB, 2022Zachary J. Brown +5 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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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
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Choledochal Cysts in the Adult
Journal of Clinical Gastroenterology, 1988Although choledochal cyst is generally considered a disorder of childhood, in approximately 20% of patients a cyst is first recognized in adult life. We reviewed nine adults who underwent operation for choledochal cyst from 1974-1985 at Yale New Haven Hospital.
C E Cahow, J P Gertler
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Archives of Pediatrics & Adolescent Medicine, 1973
Two young infants were found to have choledochal cyst. In the first patient, the only clinical manifestation was asymptomatic hepatosplenomegaly. She developed bilious ascites after a percutaneous liver biopsy. The second patient presented with fluctuating jaundice and spontaneous perforation of the cyst resulting in bilious ascites.
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Two young infants were found to have choledochal cyst. In the first patient, the only clinical manifestation was asymptomatic hepatosplenomegaly. She developed bilious ascites after a percutaneous liver biopsy. The second patient presented with fluctuating jaundice and spontaneous perforation of the cyst resulting in bilious ascites.
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