Choledochal cyst: A 14-year surgical experience with 36 patients

Author:

Tan K C1,Howard E R1

Affiliation:

1. Department of Surgery (Firm 3), King's College Hospital, Denmark Hill, London SE5 9RS, UK

Abstract

Abstract The presentation and management of 36 patients with cystic dilatation of the biliary tree seen over a 14-year period is reviewed. There were 28 females and 8 males, a ratio of 3·5:1. The classic triad of jaundice, pain and an abdominal mass was seen in only seven cases. Twelve patients suffered recurrent pancreatitis. There were three cases of variceal haemorrhage from portal hypertension secondary to biliary cirrhosis, and one case of biliary peritonitis from a ruptured cyst. Internal drainage (cystenterostomy) was performed in nine patients but five of these eventually needed cyst excision. Cysts have been excised primarily in the last 21 consecutive patients without mortality. Preliminary external drainage with T tubes was used before cyst resection in three patients who presented with complications of choledochal cysts. Cyst excision and hepaticojejunostomy is now the definitive treatment of choice.

Publisher

Oxford University Press (OUP)

Subject

Surgery

Reference49 articles.

1. Congenital choledochal cyst: with observation on rupture of the cyst and intrahepatic duct dilatation;Chen;J Pediair Surg,1973

2. Choledochal cyst: a report of 9 cases and review of the literature;Lee;Arch Surg,1969

3. Congenital cystic dilatation of the common bile duct: report of 3 cases, analysis of 57 cases and review of the literature;Tsardakas;Arch Surg,1956

4. Choledochal cyst: etiological consideration and surgical management in 22 cases;Kimura;Arch Surg,1978

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