Publication Name	World Journal of Gastroenterology
Manuscript ID	32997
Country	Germany

Received	2017-02-03 15:11
Peer-Review Started	2017-02-04 07:55
To Make the First Decision	2017-02-23 10:28
Return for Revision	2017-02-27 15:19
Revised	2017-03-11 05:33
Second Decision	2017-04-11 17:22
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2017-04-12 18:17
Articles in Press	2017-04-12 18:17
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2017-04-20 11:49
Publish the Manuscript Online	2017-04-28 10:26

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/by-nc/4.0/
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Category	Gastroenterology & Hepatology
Manuscript Type	Case Report
Article Title	Protein-losing pseudomembranous colitis with cap polyposis-like features
Manuscript Source	Invited Manuscript
All Author List	Wolfgang Kreisel, Guenther Ruf, Richard Salm, Adhara Lazaro, Bertram Bengsch, Anna-Maria Globig, Paul Fisch, Silke Lassmann and Annette Schmitt-Graeff
Funding Agency and Grant Number
Corresponding Author	Wolfgang Kreisel, MD, Professor, Department of Medicine II, Gastroenterology, Hepatology, Endocrinology and Infectious Diseases, Medical Center, University of Freiburg, Faculty of Medicine, University of Freiburg, Hugstetter Str. 55, 79106 Freiburg, Germany. wolfgang.kreisel@uniklinik-freiburg.de
Key Words	Protein-losing enteropathy; Cap polyposis; Ulcerative colitis; Goblet cells; Pseudomembranes
Core Tip	Protein-losing enteropathy (PLE) is characterized by loss of serum proteins into the gastrointestinal tract. The small intestine is the most common site of protein loss. This is an unusual case of severe PLE involving the sigmoid colon and the rectum. Surgical resection was performed and subsequent histologic evaluation confirmed a diagnosis of a pseudomembranous colitis with cap polyposis-like features.
Publish Date	2017-04-28 10:26
Citation	Kreisel W, Ruf G, Salm R, Lazaro A, Bengsch B, Globig AM, Fisch P, Lassmann S, Schmitt-Graeff A. Protein-losing pseudomembranous colitis with cap polyposis-like features. World J Gastroenterol 2017; 23(16): 3003-3010
URL	http://www.wjgnet.com/1007-9327/full/v23/i16/3003.htm
DOI	http://dx.doi.org/10.3748/wjg.v23.i16.3003

Full Article (PDF)	WJG-23-3003.pdf
Full Article (Word)	WJG-23-3003.doc
Manuscript File	32997-Review.docx
Audio Core Tip	32997-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	32997-Conflict-of-interest statement.pdf
Copyright License Agreement	32997-Copyright assignment.pdf
Signed Informed Consent Form(s) or Document(s)	32997-Informed consent statement.pdf
Institutional Review Board Approval Form or Document	32997-Institutional review board statement.pdf
Peer-review Report	32997-Peer-review(s).pdf
Scientific Misconduct Check	32997-Scientific misconduct check.pdf
Scientific Editor Work List	32997-Scientific editor work list.pdf