Publication Name	World Journal of Clinical Pediatrics
Manuscript ID	20172
Country	Thailand

Received	2015-05-29 17:11
Peer-Review Started	2015-06-02 08:45
To Make the First Decision	2015-07-03 16:45
Return for Revision	2015-07-10 19:40
Revised	2015-07-21 01:02
Second Decision	2015-09-21 17:44
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2015-09-30 18:42
Articles in Press	2015-09-30 18:42
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2015-10-21 12:11
Publish the Manuscript Online	2015-11-10 12:29

ISSN	2219-2808 (online)
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/
Copyright	© The Author(s) 2015. Published by Baishideng Publishing Group Inc. All rights reserved.
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Website	http://www.wjgnet.com

Category	Pediatrics
Manuscript Type	Review
Article Title	Current management of pediatric soft tissue sarcomas
Manuscript Source	Invited Manuscript
All Author List	Surasak Sangkhathat
Funding Agency and Grant Number	Funding Agency Grant Number Anandamahidol Foundation
Corresponding Author	Surasak Sangkhathat, MD, PhD, Department of Surgery and Tumor Biology Research Unit, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand. surasak.sa@psu.ac.th
Key Words	Pediatric tumor; Rhabdomyosarcoma; Soft tissue sarcoma; Non-rhabdomyosarcoma pediatric soft tissue tumor
Core Tip	The manuscript describes current management of pediatric soft tissue sarcomas, a large group of rare tumors in pediatric age group. The group has two main categories; rhabdomyosarcoma (RMS) and non-RMS pediatric soft tissue tumors. Treatment of these tumors is in multidisciplinary fashion comprising of surgery, chemotherapy and radiation therapy. Decision making in management protocol for each patient is based on the risk determined by various clinical and pathological parameters. For cases with low-risk, surgical removal is usually adequate when adjuvant chemoradiation are proven helpful in cases with significant risk of recurrence. The overall survival in these tumors has become brighter in the recent decades.
Publish Date	2015-11-10 12:29
Citation	Sangkhathat S. Current management of pediatric soft tissue sarcomas. World J Clin Pediatr 2015; 4(4): 94-105
URL	http://www.wjgnet.com/2219-2808/full/v4/i4/94.htm
DOI	http://dx.doi.org/10.5409/wjcp.v4.i4.94

Full Article (PDF)	WJCP-4-94.pdf
Full Article (Word)	WJCP-4-94.doc
Manuscript File	20172-Review.docx
Answering Reviewers	20172-Answering reviewers.pdf
Audio Core Tip	20172-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	20172-Conflict-of-interest statement.pdf
Copyright License Agreement	20172-Copyright assignment.pdf
Non-Native Speakers of English Editing Certificate	20172-Language certificate.pdf
Peer-review Report	20172-Peer-review(s).pdf
Scientific Misconduct Check	20172-Scientific misconduct check.pdf
Scientific Editor Work List	20172-Scientific editor work list.pdf