Imaging: ERCP View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2018-08-01

AUTHORS

Atsushi Kanno , Atsushi Masamune , Tooru Shimosegawa

ABSTRACT

Further insights into autoimmune pancreatitis (AIP) have been revealed by many researchers since a report by Yoshida et al. in 1995 [1]. Bile duct stricture accompanied by AIP has been considered as IgG4-related sclerosing cholangitis (IgG4-SC) based on several reports [2, 3]. Recently, IgG4-SC is regarded as a manifestation of a systemic IgG4-related disease (IgG4-RD) [4]. The diagnosis of IgG4-SC is based on the clinical diagnostic criteria of IgG4-related sclerosing cholangitis 2012 [5]. The clinical symptoms of IgG4-SC are similar to those of AIP. IgG4-SC is often observed in patients aged 60 years or older; it is more common in males, is associated with elevated levels of serum IgG4, and responds well to steroids. A progressive course, such as that observed in cases of primary sclerosing cholangitis (PSC), is rare, and the short-term prognosis is extremely favorable. However, the long-term prognosis for IgG4-SC remains unclear. Accurate diagnosis of IgG4-SC is essential for proper management of this disease. We present bile duct images using endoscopic retrograde cholangiopancreatography (ERCP) in cases of IgG4-SC. More... »

PAGES

63-70

Book

TITLE

IgG4-Related Sclerosing Cholangitis

ISBN

978-981-10-4547-9
978-981-10-4548-6

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-981-10-4548-6_10

DOI

http://dx.doi.org/10.1007/978-981-10-4548-6_10

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1105926813


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