Autoimmune pancreatitis: an update

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ID: 261569
2019
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Abstract
Since the time of inception of autoimmune pancreatitis (AIP), our knowledge of autoimmune pancreatitis has expanded significantly. The aim of this review is to provide an update on clinical manifestations, diagnosis, imaging features, and treatment of AIP. Type 1 AIP is the pancreatic manifestation of IgG4-related systemic disease, which can be diagnosed using a combination of clinical, histopathological, pancreatic imaging findings in conjunction with manifestation in other organs, as well of responsiveness to steroid treatment. It is vital to differentiate AIP from pancreatic cancer since both can mimic each other clinically and radiologically. Type 2 AIP is a rare but distinct subtype of AIP which occurs mostly in the younger patient. AIP is steroid-responsive chronic pancreatitis with distinct manifestations on imaging.
Reference Key
khandelwal2019abdominalautoimmune Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Ashish Khandelwal;Dai Inoue;Naoki Takahashi;Ashish Khandelwal;Dai Inoue;Naoki Takahashi;
Journal abdominal radiology
Year 2019
DOI
doi:10.1007/s00261-019-02275-x
URL
https://link.springer.com/article/10.1007/s00261-019-02275-x
Keywords
hepatology gastroenterology imaging / radiology

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