Literature DB >> 26694138

Epidemiology, clinical presentation, diagnosis and treatment of autoimmune pancreatitis: A retrospective analysis of 53 patients.

Sebastian Rasch1, Veit Phillip2, Roland M Schmid2, Hana Algül2.   

Abstract

BACKGROUND: Most of the data about epidemiology, clinical presentation and treatment of autoimmune pancreatitis (AIP) is based on case series or small study groups. We therefore analyzed all cases of AIP treated at our clinic retrospectively.
METHODS: We searched our clinical database for the diagnosis pancreatitis between January 2007 and June 2014, selected patients with AIP and entered all relevant information in a database for statistical analysis.
RESULTS: In total 53 patients with AIP were treated at our institution, 62% with type 1 and 23% with type 2 AIP. Gender distribution was male/female 3.1:1 for type 1 and 1:1.2 for type 2 AIP. The median age was 63.0 and 32.5 years for type 1 and type 2 AIP, respectively. The most common symptom is abdominal pain particular in patients with type 2 AIP whereas jaundice was only apparent in patients with type 1 AIP. The international diagnostic criteria seem to facilitate diagnosis of AIP as unnecessary pancreatic surgery in patients with AIP decreases. In 62.6% of the patients therapy was indicated and 84.8% showed a response to initial therapy with steroids. Recurring disease occurred in 28.3% of the cases but only 3.8% suffered a second relapse. Permanent maintenance therapy with steroids or additional therapy with immunomodulatory drugs is successful in recurring disease.
CONCLUSION: Our data further corroborate previous findings on epidemiology, clinical presentation and treatment of AIP. AIP is a well manageable autoimmune disease in most patients. Better biopsy techniques and simplified diagnostic criteria might further alleviate diagnosis of AIP.
Copyright © 2015 IAP and EPC. Published by Elsevier India Pvt Ltd. All rights reserved.

Entities:  

Keywords:  Autoimmune pancreatitis; Chronic pancreatitis; Idiopathic duct centric pancreatitis; IgG4; IgG4-related disease; Lymphoplasmacytic sclerosing pancreatitis

Mesh:

Year:  2015        PMID: 26694138     DOI: 10.1016/j.pan.2015.11.006

Source DB:  PubMed          Journal:  Pancreatology        ISSN: 1424-3903            Impact factor:   3.996


  7 in total

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4.  Outcome and Genetic Factors in IgG4-Associated Autoimmune Pancreatitis and Cholangitis: A Single Center Experience.

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5.  Unraveling the relationship between autoimmune pancreatitis type 2 and inflammatory bowel disease: Results from two centers and systematic review of the literature.

Authors:  Sara Nikolic; Marco Lanzillotta; Nikola Panic; Torkel B Brismar; Carlos Fernández Moro; Gabriele Capurso; Emanuel Della Torre; J-Matthias Löhr; Miroslav Vujasinovic
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6.  Clinical profile and treatment outcomes in autoimmune pancreatitis: a report from North India.

Authors:  Surinder S Rana; Rajesh Gupta; Ritambhra Nada; Pankaj Gupta; Rajinder Basher; Bhagwat R Mittal; Ravi Kumar Sharma; Amit Rawat
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7.  The Clinical Phenotype of Chinese Patients With Autoimmune Pancreatitis Differs Significantly From Western Patients.

Authors:  Qiwen Jin; Yongpeng Ge; Xixia Chen; Chang Tan; Zhenguo Huang; Bei Wang; Bo Zhang; Qinglin Peng; Xiaodi Wang; Guochun Wang
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  7 in total

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