Autoimmune Pancreatitis Type 2: Case Report

Author:

Onweni Chidinma1,Balagoni Harika1,Treece Jennifer M.1,Addo Yobo Emmanuel1,Patel Archi1,Phemister Jennifer12,Srinath Manoj12,Young Mark F.12

Affiliation:

1. East Tennessee State University, Johnson City, TN, USA

2. James H. Quillen Veterans Affairs Medical Center, Mountain Home, TN, USA

Abstract

A middle-aged man presents with acute pancreatitis of unknown etiology and is found to have a presentation consistent with the diagnosis of type 2 autoimmune pancreatitis (AIP). AIP is a group of rare heterogeneous diseases that are challenging to diagnose. There are 2 types of AIP. Type 1 disease is the more common worldwide than type 2 AIP. While type 1 AIP is associated with IgG4-positive antibodies, type 2 AIP is IgG4 antibody negative. Both types of AIP are responsive to corticosteroid treatment. Although type 1 AIP has more extrapancreatic manifestations and more commonly relapses, this is a case of a patient with type 2 AIP with inflammatory bowel disease and relapsing course.

Publisher

SAGE Publications

Subject

Safety Research,Safety, Risk, Reliability and Quality,Epidemiology

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