Choledochal Cyst Disease A Changing Pattern of Presentation
- 1 November 1994
- journal article
- research article
- Published by Wolters Kluwer Health in Annals of Surgery
- Vol. 220 (5) , 644-652
- https://doi.org/10.1097/00000658-199411000-00007
Abstract
The authors compared the presentation, treatment, and long-term outcome of children and adults with choledochal cysts. The typical patient with choledochal cyst disease has been the female infant with the triad of jaundice, an abdominal mass, and pain. However, the recent experience of the authors suggested that the disease currently is recognized more commonly in adults. Forty-two patients (11 children, 32 adults) with choledochal cyst disease were treated primarily at this institution between 1976 and 1993. Patients presentation, clinical evaluation, and operative treatment were obtained from existing records. Long-term follow-up was obtained by records, physician, or direct patient contact. One child--but no adults--had the classic triad of jaundice, abdominal mass, and pain. Children were more likely to have two of the three signs or symptoms (82% vs. 25%; p = < 0.05). Adult patients most commonly had abdominal pain and were thought to have pancreatitis (23%) or acute biliary tract symptoms, prompting cholecystectomy (50%). The type of choledochal cyst seen in children and adults was similar; the fusiform extrahepatic (Type I) was most common (50%), and the combined intrahepatic and extrahepatic (Type IVA) was the next most prominent (33%). For both children and adults, treatment consisted of excision of the cyst and biliary reconstruction with a hepaticojejunostomy. There was no surgical mortality. Gallbladder or cholangiocarcinoma was identified in three adults (9.7%), two of which were manifest on presentation. Long-term follow-up revealed one patient with a biliary stricture and three patients with Type IVA cysts who had intrahepatic stones. Children and adults differ in presentation of choledochal cysts, with adults commonly having acute biliary tract or pancreatic symptoms. Surgical treatment with cysts excision and biliary bypass is safe and effective in children and adults with excellent long-term results that minimize the development of malignancy.Keywords
This publication has 24 references indexed in Scilit:
- Biliary papillomatosis with the point mutation of K-ras gene arising in congenital choledochal cystGastroenterology, 1993
- Choledochal duct cyst: resection with physiologic reconstruction.1992
- Congenital Choledochal Dilatation With Emphasis on Pathophysiology of the Biliary TractAnnals of Surgery, 1992
- Variation in management based on type of choledochal cystThe American Journal of Surgery, 1991
- Surgical techniques and long-term results in the treatment of choledochal cystJournal of Pediatric Surgery, 1990
- Congenital biliary dilatation: a spectrum of disease detailed by ultrasoundThe British Journal of Radiology, 1990
- Management of Bile Duct Cysts in AdultsArchives of Surgery, 1986
- Abnormalities of the Pancreatic and Biliary Ducts in Adult Patients With Choledochal CystsArchives of Surgery, 1983
- Carcinoma arising in the wall of congenital bile duct cystsCancer, 1979
- Management of Congenital Choledochal Cyst with Intrahepatic InvolvementAnnals of Surgery, 1978