Publication Name	World Journal of Clinical Cases
Manuscript ID	57373
Country	China

Received	2020-07-12 08:07
Peer-Review Started	2020-07-12 08:08
To Make the First Decision
Return for Revision	2020-09-24 21:50
Revised	2020-10-02 08:58
Second Decision	2020-10-26 11:07
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2020-10-26 21:36
Articles in Press	2020-10-26 21:36
Publication Fee Transferred
Edit the Manuscript by Language Editor	2020-11-04 00:08
Typeset the Manuscript	2020-12-01 06:16
Publish the Manuscript Online	2020-12-04 09:56

ISSN	2307-8960 (online)
Open Access	This article 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 NonCommercial (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/
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Category	Oncology
Manuscript Type	Case Report
Article Title	Small-cell neuroendocrine carcinoma of the rectum — a rare tumor type with poor prognosis: A case report and review of literature
Manuscript Source	Unsolicited Manuscript
All Author List	Zhen-Zhou Chen, Wang Huang and Zheng-Qiang Wei
ORCID	Author(s) ORCID Number Zhen-Zhou Chen http://orcid.org/0000-0002-4324-5388 Wang Huang http://orcid.org/0000-0002-5634-1272 Zheng-Qiang Wei http://orcid.org/0000-0002-6499-6033
Funding Agency and Grant Number
Corresponding Author	Zheng-Qiang Wei, MD, Doctor, Doctor, Lecturer, Department of Gastrointestinal Surgery, The First Affiliated Hospital of Chongqing Medical University, No. 1 Youyi Road, Yuanjiagang, Chongqing 400000, China. 384535713@qq.com
Key Words	Case report; Small-cell neuroendocrine carcinoma; Rectum; Treatment; Prognosis; Rare tumor
Core Tip	Total mesorectal excision was performed, according to pathological analysis, and R0 resection was achieved. However, this patient had tumor recurrence only one month after surgery. Therefore, small-cell neuroendocrine carcinoma of the rectum is a high-grade carcinoma with an aggressive phenotype.
Publish Date	2020-12-04 09:56
Citation	Chen ZZ, Huang W, Wei ZQ. Small-cell neuroendocrine carcinoma of the rectum — a rare tumor type with poor prognosis: A case report and review of literature. World J Clin Cases 2020; 8(23): 6095-6102
URL	https://www.wjgnet.com/2307-8960/full/v8/i23/6095.htm
DOI	https://dx.doi.org/10.12998/wjcc.v8.i23.6095

Full Article (PDF)	WJCC-8-6095.pdf
Full Article (Word)	WJCC-8-6095.docx
CARE Checklist–2016	57373-CARE-Checklist–2016-revision.pdf
Manuscript File	57373-Review-Filipodia.docx
Answering Reviewers	57373-Answering reviewers.pdf
Audio Core Tip	57373-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	57373-Conflict-of-interest statement.pdf
Copyright License Agreement	57373-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	57373-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	57373-Language certificate.pdf
Peer-review Report	57373-Peer-review(s).pdf
Scientific Misconduct Check	57373-Bing-Wang JL-1.jpg
Scientific Misconduct Check	57373-Scientific misconduct check.pdf
Scientific Editor Work List	57373-Scientific editor work list.pdf
CrossCheck Report	57373-CrossCheck report.pdf