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©The Author(s) 2015. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Pharmacol Ther. Nov 6, 2015; 6(4): 199-206
Published online Nov 6, 2015. doi: 10.4292/wjgpt.v6.i4.199
Autoimmune pancreatitis and cholangitis
Niraj Jani, James Buxbaum
Niraj Jani, James Buxbaum, Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033-1370, United States
Author contributions: Jani N and Buxbaum J contributed equally to this work; they performed a comprehensive chronological review of this topic, prepared the figures, and wrote the paper.
Conflict-of-interest statement: The authors declare no conflict of interest.
Correspondence to: James Buxbaum, MD, Division of Gastrointestinal and Liver Diseases, Keck School of Medicine, University of Southern California, D and T Building Room B4H100, 1983 Marengo Street, Los Angeles, Ca 90033-1370, United States. jbuxbaum@usc.edu
Telephone: +1-323-4095371 Fax: +1-323-4418352
Received: April 28, 2015
Peer-review started: May 6, 2015
First decision: June 2, 2015
Revised: June 22, 2015
Accepted: August 25, 2015
Article in press: August 31, 2015
Published online: November 6, 2015
Processing time: 198 Days and 11.2 Hours
Core Tip

Core tip: Autoimmune pancreatitis is a component of a systemic immunoglobulin G subtype-4 mediated disease which also impacts the bile duct, salivary glands, kidney, and numerous other sites. It presents with jaundice and pancreas mass but it responds promptly to steroids and immunomodulators. A careful diagnostic approach is mandatory as autoimmune pancreatitis and its biliary manifestations closely resemble pancreas cancer and primary sclerosing cholangitis, diseases which have a more ominous course.