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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
R, Gupta +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
R, Gupta +3 more
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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.
Sean M, Ronnekleiv-Kelly +3 more
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Archives of Surgery, 1984
To the Editor.—Rattner et al1have stated that "mucosal abnormalities have been described only in adults," suggesting that choledochal cysts in children might represent a different pathologic entity from those found in adults. Our review of 19 cases of choledochal cysts in children reported that the cyst walls "showed fibrous tissue, fragmented elastic
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To the Editor.—Rattner et al1have stated that "mucosal abnormalities have been described only in adults," suggesting that choledochal cysts in children might represent a different pathologic entity from those found in adults. Our review of 19 cases of choledochal cysts in children reported that the cyst walls "showed fibrous tissue, fragmented elastic
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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.
J P, Gertler, C E, Cahow
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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 ...
K, Muakkasah, S, Obeid, M, Slim
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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 ...
K, Muakkasah, S, Obeid, M, Slim
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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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Choledochal Cyst Excision in Infants—A Retrospective Study
Children, 2023Grzegorz Kowalewski +2 more
exaly