| Literature DB >> 20431770 |
Eun Sun Kim1, Yoon Tae Jeen, Bora Keum, Yeon Seok Seo, Hoon Jai Chun, Soon Ho Um, Chang Duck Kim, Ho Sang Ryu.
Abstract
Cap polyposis is a rare disorder with characteristic endoscopic and histological features; its etiology is still unknown, and no specific treatment has been established. We report a case of cap polyposis that improved remarkably after infliximab infusion and had no recurrence for 3 years.Entities:
Keywords: Cap polyposis; Infliximab; Long term follow up; Therapeutics
Year: 2009 PMID: 20431770 PMCID: PMC2852720 DOI: 10.5009/gnl.2009.3.4.325
Source DB: PubMed Journal: Gut Liver ISSN: 1976-2283 Impact factor: 4.519