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Congenital Choledochal Cysts

Kamel Muakkasah, MD; Sami Obeid, MD; Michel Slim, MD
Arch Surg. 1976;111(10):1112-1114. doi:10.1001/archsurg.1976.01360280070011.
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• Cystic dilation of the common bile duct is a rare congenital anomaly. The cases of two patients, 2½ 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 operation. A follow-up of three years after cystoduodenostomy and 14 years after a hepaticojejunostomy is reported. In infants and small children, a cystoduodenostomy is usually done; otherwise, a cystojejunostomy should be the preferred initial operation. Excision may be attempted if the cyst is very small, and in selected cases.

(Arch Surg 111:1112-1114, 1976)


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