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Published in: Current Treatment Options in Gastroenterology 4/2017

01-12-2017 | Pancreas (V Chandrasekhara, Section Editor)

Diagnosis and Management of Autoimmune Pancreatitis

Authors: Phil A. Hart, MD, Somashekar G. Krishna, MD, MPH, Kazuichi Okazaki, MD

Published in: Current Treatment Options in Gastroenterology | Issue 4/2017

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Opinion statement

Although autoimmune pancreatitis is a relatively uncommon pancreatic disorder, it is an important consideration in the differential diagnosis of jaundice and pancreatic masses to avoid unnecessary surgical resection. The clinical diagnosis of autoimmune pancreatitis involves considering multiple pieces of information including the pancreatic imaging, serum IgG4 level, presence of characteristic other involvement, and histologic findings. Unlike other pancreatic disorders, this condition rapidly responds to treatment with steroids. In the more common disease subtype (type 1 autoimmune pancreatitis) disease relapses can occur necessitating the use of maintenance treatment with low-dose steroids, steroid-sparing immunomodulators, or rituximab. This chapter reviews the diagnosis and treatment of the autoimmune pancreatitis subtypes.
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Metadata
Title
Diagnosis and Management of Autoimmune Pancreatitis
Authors
Phil A. Hart, MD
Somashekar G. Krishna, MD, MPH
Kazuichi Okazaki, MD
Publication date
01-12-2017
Publisher
Springer US
Published in
Current Treatment Options in Gastroenterology / Issue 4/2017
Print ISSN: 1092-8472
Electronic ISSN: 1534-309X
DOI
https://doi.org/10.1007/s11938-017-0147-x

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