Publication Name	World Journal of Gastroenterology
Manuscript ID	31107
Country	United States

Received	2016-10-30 15:07
Peer-Review Started	2016-10-30 21:12
To Make the First Decision	2016-12-19 11:01
Return for Revision	2016-12-20 11:14
Revised	2016-12-23 07:15
Second Decision	2016-12-29 10:50
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2017-01-04 16:32
Articles in Press	2017-01-04 16:32
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2017-03-20 16:52
Publish the Manuscript Online	2017-04-06 18:30

ISSN	1007-9327 (print) and 2219-2840 (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/bync/4.0/
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Category	Gastroenterology & Hepatology
Manuscript Type	Case Report
Article Title	Hepatic angiosarcoma with clinical and histological features of Kasabach-Merritt syndrome
Manuscript Source	Unsolicited Manuscript
All Author List	Sanya Wadhwa, Tae Hun Kim, Leah Lin, Gary Kanel and Takeshi Saito
Funding Agency and Grant Number
Corresponding Author	Takeshi Saito, MD, PhD, Department of Medicine, Molecular Microbiology and Immunology, and Pathology, Division of Gastrointestinal and Liver Diseases, Keck School of Medicine of USC, University of Southern California, 2011 Zonal Avenue, HMR 801A, Los Angeles, CA 9003, United States. saitotak@usc.edu
Key Words	Hepatic angiosarcoma; Kasabach-Merritt syndrome; Vascular tumor
Core Tip	Kasabach-Merritt syndrome (KMS) is characterized by thrombocytopenia and hyper­consumption of coagulation factors within a vascular tumor. KMS is typically seen in the pediatric population however there have been reports of KMS occurring in association with adult vascular tumors. Based on laboratory findings, it is hard to differentiate KMS from disseminated intravascular coagulation. Here, we describe, for the first time the histological evidence validating the concept of KMS.
Publish Date	2017-04-06 18:30
Citation	Wadhwa S, Kim TH, Lin L, Kanel G, Saito T. Hepatic angiosarcoma with clinical and histological features of Kasabach-Merritt syndrome. World J Gastroenterol 2017; 23(13): 2443-2447
URL	http://www.wjgnet.com/1007-9327/full/v23/i13/2443.htm
DOI	http://dx.doi.org/10.3748/wjg.v23.i13.2443

Full Article (PDF)	WJG-23-2443.pdf
Full Article (Word)	WJG-23-2443.doc
Manuscript File	31107-Review.docx
Answering Reviewers	31107-Answering reviewers.pdf
Audio Core Tip	31107-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	31107-Conflict of interest statement.pdf
Copyright License Agreement	31107-Copyright assignment.pdf
Institutional Review Board Approval Form or Document	31107-Institutional review board statement.pdf
Peer-review Report	31107-Peer-review(s).pdf
Scientific Misconduct Check	31107-Scientific misconduct check.pdf
Scientific Editor Work List	31107-Scientific editor work list.pdf