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  Vol. 111 No. 10, October 1976 TABLE OF CONTENTS
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Congenital Choledochal Cysts

Kamel Muakkasah, MD; Sami Obeid, MD; Michel Slim, MD

Arch Surg. 1976;111(10):1112-1114.


Abstract

• Cystic dilation of the common bile duct is a rare congenital anomaly. The cases of two patients, 21/2 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 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)



Author Affiliations

From the Department of Surgery, School of Medicine, American University of Beirut (Lebanon).


Footnotes

Accepted for publication March 5, 1976.

Reprints not available.



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Management Dilemmas With Choledochal Cysts
Metcalfe et al.
Arch Surg 2003;138:333-339.
ABSTRACT | FULL TEXT  





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