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Articles Published Processes
8/26/2014 2:46:00 PM | Browse: 1132 | Download: 1298
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Received |
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2014-01-16 10:48 |
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Peer-Review Started |
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2014-01-16 16:17 |
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To Make the First Decision |
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2014-02-28 17:57 |
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Return for Revision |
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2014-03-07 21:14 |
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Revised |
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2014-03-28 08:34 |
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Second Decision |
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2014-04-09 08:22 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2014-04-09 09:10 |
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Articles in Press |
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2014-05-23 09:40 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2014-06-06 13:14 |
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Publish the Manuscript Online |
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2014-06-21 13:56 |
Category |
Gastroenterology & Hepatology |
Manuscript Type |
Case Report |
Article Title |
Cronkhite-Canada syndrome: Report of six cases and review of literature
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Xiao-Heng Wen, Lan Wang, Yu-Xuan Wang and Jia-Ming Qian |
Funding Agency and Grant Number |
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Corresponding Author |
Jia-Ming Qian, Director, Department of Gastroenterology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No. 1, Shuai Fu Yuan, Beijing 100730, China. qianjiaming1957@126.com |
Key Words |
Cronkhite-Canada syndrome; Clinical feature; Etiology; Therapeutics |
Core Tip |
Cronkhite-Canada syndrome (CCS) is a rare noncongenital gastrointestinal polyposis syndrome, characterized by skin hyperpigmentation, hair loss and nail atrophy, associated with high morbidity. This case report summarizes the characteristics of six CCS patients, and reviews the literature. Comprehensive treatment led by corticosteroids can improve prognosis, and long-term follow-up is necessary. |
Publish Date |
2014-06-21 13:56 |
Citation |
Wen XH, Wang L, Wang YX, Qian JM. Cronkhite-Canada syndrome: Report of six cases and review of literature. World J Gastroenterol 2014; 20(23): 7518-7522 |
URL |
http://www.wjgnet.com/1007-9327/full/v20/i23/7518.htm |
DOI |
http://dx.doi.org/10.3748/wjg.v20.i23.7518 |
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