Case Report
Copyright ©The Author(s) 2015. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Surg. Jun 27, 2015; 7(6): 98-101
Published online Jun 27, 2015. doi: 10.4240/wjgs.v7.i6.98
Gastrointestinal stromal tumour presenting as palpable abdominal mass: A rare entity
Manoj R Bhambare, Jayashri S Pandya, Sudatta B Waghmare, Tilakdas S Shetty
Manoj R Bhambare, Jayashri S Pandya, Sudatta B Waghmare, Tilakdas S Shetty, Department of General Surgery, Topiwala National Medical College and Bai Yamunabai Laxman Nair Hospital, Mumbai 400008, India
Author contributions: All authors contributed to this manuscript.
Ethics approval: The study reviewed and waivered by the BYL Nair Hospital and T N Medical College ethics committee.
Informed consent: The study participant provided informed written consent.
Conflict-of-interest: We certify that there is no conflict of interest with any financial organisation regarding material discussed in the manuscript.
Open-Access: This article is an open-access article which 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/
Correspondence to: Dr. Jayashri S Pandya, Professor, Department of General Surgery, Topiwala National Medical College and Bai Yamunabai Laxman Nair Hospital, Mumbai Central, Mumbai 400008, India. smruti63@hotmail.com
Telephone: +91-02-223027148
Received: December 3, 2014
Peer-review started: December 7, 2014
First decision: February 7, 2015
Revised: April 16, 2015
Accepted: May 5, 2015
Article in press: May 6, 2015
Published online: June 27, 2015
Core Tip

Core tip: Gastrointestinal stromal tumours presenting with palpable abdominal mass are rare. Diagnosis is based upon histopathology and immunehistochemistry. Pre operatively patient should be evaluated with different modalities for diagnosis and resectability of tumour. Surgical resection with postoperative Imatinib chemotherapy helps to provide long term survival.