BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
1/18/2023 5:48:01 AM | Browse: 359 | Download: 1068
 |
Received |
|
2022-10-09 17:41 |
|
Peer-Review Started |
|
2022-10-09 17:42 |
|
First Decision by Editorial Office Director |
|
2022-11-03 08:20 |
|
Return for Revision |
|
2022-11-04 09:17 |
|
Revised |
|
2022-11-18 11:15 |
 |
Publication Fee Transferred |
|
|
|
Second Decision by Editor |
|
2023-01-03 03:42 |
|
Second Decision by Editor-in-Chief |
|
|
|
Final Decision by Editorial Office Director |
|
2023-01-04 18:42 |
|
Articles in Press |
|
2023-01-04 18:42 |
|
Edit the Manuscript by Language Editor |
|
2022-12-26 23:37 |
|
Typeset the Manuscript |
|
2023-01-06 06:05 |
|
Publish the Manuscript Online |
|
2023-01-18 05:48 |
| ISSN |
1948-9366 (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/ |
| Copyright |
© The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
|
| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
|
| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| Category |
Surgery |
| Manuscript Type |
Opinion Review |
| Article Title |
Hereditary polyposis syndromes remain a challenging disease entity: Old dilemmas and new insights
|
| Manuscript Source |
Invited Manuscript |
| All Author List |
Frederik Rønne Pachler, Anna Byrjalsen, John Gásdal Karstensen and Anne Marie Jelsig |
| ORCID |
|
| Funding Agency and Grant Number |
|
| Corresponding Author |
Frederik Rønne Pachler, MD, PhD, Surgeon, Danish Polyposis Registry, Gastrounit, Copenhagen University Hospital - Amager and Hvidovre Hospital, Kettegård Allé 30, Hvidovre 2650, Denmark. frederik.roenne.pachler.01@regionh.dk |
| Key Words |
Hereditary polyposis; Familial adenomatous polyposis; Juvenile polyposis syndrome; Peutz-Jegher syndrome |
| Core Tip |
Genetic technologies and testing have evolved immensely over the past decades allowing for tailored surveillance of patients with hereditary polyposis syndromes. These include endoscopic follow-up and surgery when endoscopic management is no longer possible. Chemopreventive drugs may serve as a cornerstone in future management, but it has yet to show consistent prevention of disease progression. |
| Publish Date |
2023-01-18 05:48 |
| Citation |
Pachler FR, Byrjalsen A, Karstensen JG, Jelsig AM. Hereditary polyposis syndromes remain a challenging disease entity: Old dilemmas and new insights. World J Gastrointest Surg 2023; 15(1): 1-8 |
| URL |
https://www.wjgnet.com/1948-9366/full/v15/i1/1.htm |
| DOI |
https://dx.doi.org/10.4240/wjgs.v15.i1.1 |
All content on this site: Copyright © 1993-2026 Baishideng Publishing Group Inc, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies. For all open access content, the relevant licensing terms apply.
