| Literature DB >> 21686984 |
Kazuki Nagai1, Hiroo Hosaka, Yutaka Takahashi, Shuichi Kubo, Noriko Nakamura, Kazuo Andou.
Abstract
We present a case of IgG4-related sclerosing disease complicated by sclerosing cholangitis (SC), idiopathic retroperitoneal fibrosis (IRF) and orbital pseudotumour (OPT). Clinical, radiographic and pathological findings later suggested that the patient had SC complicated by IRF. The patient's SC and IRF were well controlled for the first 10 years of the follow-up period; OPT developed in the tenth year. During investigation of the OPT, serum IgG4 level was found to be significantly elevated. The patient was then diagnosed with IgG4-related sclerosing disease complicated by SC, IRF and OPT. This is a rare manifestation of IgG4-related sclerosing disease, which was diagnosed incidentally during OPT work-up. We suggest that this is a variation of the so-called IgG4-related sclerosing disease or hyper-IgG4 disease.Entities:
Year: 2009 PMID: 21686984 PMCID: PMC3027777 DOI: 10.1136/bcr.02.2009.1590
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X