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
. 2014 Mar 18;6(1):5173.
doi: 10.4081/rt.2014.5173. eCollection 2014 Jan 23.

Robotic-assisted surgery approach in a biliary rhabdomyosarcoma misdiagnosed as choledochal cyst

Affiliations
Case Reports

Robotic-assisted surgery approach in a biliary rhabdomyosarcoma misdiagnosed as choledochal cyst

Ghassan Nakib et al. Rare Tumors. .

Abstract

Rhabdomyosarcoma is a soft tissue malignant tumor affecting 1% of children from 0 to 14 years. Preoperative imaging may not always be diagnostic for hepatobiliary rhabdomyosarcoma and differential diagnosis with choledochal cyst (CC) could be difficult. We report a case of 2-years-old girl with a strange CC pattern of presentation. A grapelike lesion involving the choledochal and biliary ducts was easily and completely resected by robotic assisted surgery. Since no previous reports were available about oncologic safety of robotic approach, the porto-enterostomy was performed in open surgery. On histologic examination, the specimen revealed a botryoidembryonal rhabdomyosarcoma affecting both the common bile duct and the common hepatic duct. One year postoperatively the child is safe of tumor relapse. Robotic approach seems to be safe and advantageous to obtain a radical excision of the tumor at the porta hepatis, even in case of misdiagnosed malignant lesion mimicking a CC.

Keywords: biliary botryoid rhabdomyosarcoma; choledochal cyst; porta hepatis; robotic surgery.

PubMed Disclaimer

Conflict of interest statement

Conflict of interests: the authors declare no potential conflict of interests.

Figures

Figure 1.
Figure 1.
Choledochal cyst imaging. A) cholangiography showing the choledochal fusiform dilatation; B) magnetic resonance imaging aspect with evidence of dilatation of biliary ducts.
Figure 2.
Figure 2.
Intraoperative features of biliary three A) extrahepatic ducts: common hepatic duct (CHD) showing grape like tumour and common bile duct (CBD); B) intrahepatic biliary ducts: right anterior and posterior (1-2) and left anterior and posterior (3-4).

Similar articles

Cited by

References

    1. Stocker JT. Hepatic tumors in children. Clin Liver Dis 2001;5:259-81 - PubMed
    1. Meyers RL. Tumors of the liver in children. Surg Oncol 2007;16:195-203 - PubMed
    1. Kebudi R, Görgun O, Ayan I, et al. Rhabdmyosarcoma of the biliary tree. Pediatr Int 2003;45:469-71 - PubMed
    1. Duan F, Smith LM, Gustafson DM, et al. Genomic and clinical analysis of fusion gene amplification in rhabdomyosarcoma: a report from the Children’s Oncology Group. Genes Chromosomes Cancer 2012; 51:662-74 - PMC - PubMed
    1. Tireli GA, Sander S, Dervisoglu S, et al. Embryonal rhabdomyosarcoma of the common bile duct mimicking choledochal cyst. J Hepatobiliary Pancreat Surg 2005;12:263-5 - PubMed

Publication types