Publication Name	World Journal of Clinical Cases
Manuscript ID	24881
Country	South Korea

Received	2016-02-14 10:10
Peer-Review Started	2016-02-14 14:18
To Make the First Decision	2016-03-30 11:46
Return for Revision	2016-03-30 16:18
Revised	2016-04-24 18:41
Second Decision	2016-05-09 18:20
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2016-05-27 11:12
Articles in Press	2016-05-27 11:12
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2016-07-25 09:03
Publish the Manuscript Online	2016-08-12 18:39

ISSN	2307-8960 (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) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
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Category	Gastroenterology & Hepatology
Manuscript Type	Case Report
Article Title	Primary hepatic neuroendocrine tumor: A case report and literature review
Manuscript Source	Unsolicited Manuscript
All Author List	Jeong Eun Song, Byung Seok Kim and Chang Hyeong Lee
Funding Agency and Grant Number
Corresponding Author	Chang Hyeong Lee, MD, PhD, Professor, Department of Internal Medicine, Catholic University of Daegu School of Medicine, 33, Duryugongwon-ro 17-gil, Nam-gu, Daegu 42472, South Korea. chlee1@cu.ac.kr
Key Words	Primary hepatic neuroendocrine tumor; Neuroendocrine tumor; Liver; Hepatocelluar carcinoma
Core Tip	Primary hepatic neuroendocrine tumors (PHNETs) are extremely rare and difficult to diagnose before preoperative biopsy or surgery. This case report shows that the diagnosis of PHNET is a medical challenge. Thus differentiation of PHNET from other hepatic mass and exclusion of occult primary neuroendocrine tumors are necessary. The diagnosis of PHNET can be ascertained after long term follow-up to exclude another primary origin.
Publish Date	2016-08-12 18:39
Citation	Song JE, Kim BS, Lee CH. Primary hepatic neuroendocrine tumor: A case report and literature review. World J Clin Cases 2016; 4(8): 243-247
URL	http://www.wjgnet.com/2307-8960/full/v4/i8/243.htm
DOI	http://dx.doi.org/10.12998/wjcc.v4.i8.243

Full Article (PDF)	WJCC-4-243.pdf
Full Article (Word)	WJCC-4-243.doc
Manuscript File	24881-Edited-1.docx
Answering Reviewers	Author Response Letter to Reviewer Comments.docx
Audio Core Tip	24881_audio core tip.mp3
Copyright License Agreement	24881_copyright assignment.pdf
Institutional Review Board Approval Form or Document	IRB certification.pdf
Non-Native Speakers of English Editing Certificate	Language certification.pdf
Peer-review Report	24881-Peer-review(s).pdf
Scientific Editor Work List	24881-Scientific editor work list.pdf