Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2022 Mar 30;2022(3):rjac126.
doi: 10.1093/jscr/rjac126. eCollection 2022 Mar.

Choledochal cysts type VI: biliary cyst of the cystic duct with connecting to right anterior sectoral bile duct: a case report

Affiliations
Case Reports

Choledochal cysts type VI: biliary cyst of the cystic duct with connecting to right anterior sectoral bile duct: a case report

Nattaporn Maneepairoj et al. J Surg Case Rep. .

Abstract

Type VI choledochal cysts or cystic duct dilatation cysts are a relatively new and rare condition. We report the case of a 35-year-old man who presented with a history of recurrent episodes of epigastrium pain. Magnetic resonance cholangiography revealed a cyst lodged between the cystic duct and the right anterior sectoral bile duct. He underwent a laparoscopic right anterior sectorectomy with cholecystectomy. Pathological examination revealed a cyst with a fibrous wall, dense chronic inflammatory infiltration, lined by columnar epithelium. Due to its rarity, the diagnosis is often made intraoperatively. The treatment of cystic duct cysts includes cholecystectomy, complete cyst excision, recontinuity of the common bile duct. Type VI choledochal cysts are extremely rare. Preoperative diagnosis, using either magnetic resonance cholangiopancreatography or endoscopic retrograde cholangiopancreatography, is vital to prevent postoperative complications. Treatment of this type of cysts includes cholecystectomy and complete cyst excision and biliary-enteric reconstruction if necessary.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Computed tomography image showing an intrahepatic cyst (arrow).
Figure 2
Figure 2
MRCP showing a cyst connected to the cystic duct (arrow) and the right anterior sectoral bile duct (arrowhead).
Figure 3
Figure 3
ERCP showing that the cyst can be filled with contrast from the cystic duct (arrow) and the right anterior sectoral bile duct (arrowhead).
Figure 4
Figure 4
[Left] the surgical specimen revealed that the lumen of the cyst was connected to the right anterior sectoral bile duct (arrow) and the cystic duct (arrowhead). [right] Diagram of the cystic duct cyst.
Figure 5
Figure 5
Pathological examination revealed a cyst with a fibrous wall (arrow), dense chronic inflammatory infiltration, lined by columnar epithelium (arrowhead). Mild reactive atypia, associated with marked chronic inflammatory cell infiltration, was noted. No signs of epithelial dysplasia were observed.

References

    1. Todani T, Watanabe Y, Narusue M, Tabuchi K, Okajima K. Congenital bile duct cysts: classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst. Am J Surg 1977;134:263–9. - PubMed
    1. Serradel AFS, Linares ES, Goepfert RH. Cystic dilatation of the cystic duct: a new type of biliary cyst. Surgery 1991;109:320–2. - PubMed
    1. Bode WE, Aust JB. Isolated cystic dilatation of the cystic duct. Am J Surg 1983;145:828–9. - PubMed
    1. De U, Das S, Sarkar S. Type VI choledochal cyst revisited. Singapore Med J 2011;52:e91–3. - PubMed
    1. Bheerappa N, Sastry RA. Pancreatico-biliary ductal union. Trop Gastroenterol 2001;22:190–3. - PubMed

Publication types