Publication Name	World Journal of Hepatology
Manuscript ID	52999
Country	China

Received	2019-11-28 14:30
Peer-Review Started	2019-11-28 14:31
To Make the First Decision	2020-01-15 03:13
Return for Revision	2020-01-17 07:35
Revised	2020-02-06 06:39
Second Decision	2020-02-27 11:08
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2020-03-01 23:03
Articles in Press	2020-03-01 23:03
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2020-03-18 03:16
Publish the Manuscript Online	2020-03-24 05:16

ISSN	1948-5182 (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) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.
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Category	Gastroenterology & Hepatology
Manuscript Type	Review
Article Title	Polycystic liver disease: Classification, diagnosis, treatment process, and clinical management
Manuscript Source	Invited Manuscript
All Author List	Ze-Yu Zhang, Zhi-Ming Wang and Yun Huang
ORCID	Author(s) ORCID Number Ze-Yu Zhang http://orcid.org/0000-0003-0505-3112 Zhi-Ming Wang http://orcid.org/0000-0003-3145-8981 Yun Huang http://orcid.org/0000-0001-8517-0516
Funding Agency and Grant Number
Corresponding Author	Yun Huang, MD, PhD, Professor, Department of Hepatobiliary Surgery, Xiangya Hospital, Central South University, No. 87 Xiangya Road, Changsha 410000, Hunan Province, China. huangyun-1002@163.com
Key Words	Polycystic liver disease; Autosomal dominant polycystic kidney disease; Autosomal recessive polycystic kidney disease; Isolated polycystic liver disease; Diagnosis; Treatment
Core Tip	Polycystic liver disease (PLD) is a rare hereditary disease. However, there is no unified strategy in the treatment of PLD so far. In order to better understand recent progresses on clinical practice of PLD and contribute to potential directions for future researches, we conducted this review mainly focusing on recent progresses of PLD classification, clinical manifestation, diagnosis and treatments. For information, we also provided medical treatment process of PLD that is being used in our medical center.
Publish Date	2020-03-24 05:16
Citation	Zhang ZY, Wang ZM, Huang Y. Polycystic liver disease: Classification, diagnosis, treatment process, and clinical management. World J Hepatol 2020; 12(3): 72-83
URL	https://www.wjgnet.com/1948-5182/full/v12/i3/72.htm
DOI	https://dx.doi.org/10.4254/wjh.v12.i3.72

Full Article (PDF)	WJH-12-72.pdf
Full Article (Word)	WJH-12-72.docx
Manuscript File	52999-Review.docx
Answering Reviewers	52999-Answering reviewers.pdf
Audio Core Tip	52999-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	52999-Conflict-of-interest statement.pdf
Copyright License Agreement	52999-Copyright license agreement.pdf
Non-Native Speakers of English Editing Certificate	52999-Language certificate.pdf
Peer-review Report	52999-Peer-review(s).pdf
Scientific Misconduct Check	52999-Scientific misconduct check.pdf
Scientific Editor Work List	52999-Scientific editor work list.pdf