Case Report
Copyright ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Surg. Nov 27, 2019; 11(11): 414-421
Published online Nov 27, 2019. doi: 10.4240/wjgs.v11.i11.414
Pediatric intrahepatic bile duct adenoma - rare liver tumor: A case report
Anup Kumar Roy, Nrityen Nath Das
Anup Kumar Roy, Department of Surgery, Downtown Hospital, Guwahati, Assam 781006, India
Nrityen Nath Das, Hepato-biliary and Liver Transplant Center, Downtown Hospital, Guwahati, Assam 781006, India
Author contributions: Roy AK and Das NN contributed equally to this work in all aspects, from conception to writing of the manuscript.
Informed consent statement: Informed consent was obtained from the patient.
Conflict-of-interest statement: To the best of our knowledge, no conflict of interest exists.
CARE Checklist (2016) statement: The authors have checked the manuscript according to the checklist.
Open-Access: This is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Corresponding author: Anup Kumar Roy, MBBS, Doctor, Department of Surgery, Downtown Hospital, G. S. Road, Guwahati, Assam 781006, India. roy.anup1@gmail.com
Telephone: +91-96-5096-0564
Received: July 4, 2019
Peer-review started: July 16, 2019
First decision: August 2, 2019
Revised: September 7, 2019
Accepted: September 25, 2019
Article in press: September 25, 2019
Published online: November 27, 2019
Processing time: 145 Days and 19.4 Hours
Core Tip

Core tip: Intrahepatic bile duct adenoma is a rare tumor arising from bile ductules in the liver. It is mostly seen as an incidental finding in adults but it is almost unheard of in children. Therefore it is one of the rarest tumors in children. Although it is a benign tumor, it has the potential to be malignant according to one study reported in adults. This case highlights the fact that it is the second case of this rare tumor occurring in the pediatric age group in the world. The progression into a large tumor in our case report necessitates the need for more information on this rare tumor.