2021
DOI: 10.1002/jgh3.12688
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Autoimmune pancreatitis: What we know so far

Abstract: Autoimmune pancreatitis (AIP) is a rare, often‐missed disease that involves inflammation of the pancreas and strictures of the pancreatic duct. Its prevalence and incidence in the United States remain scarce. The disease has a varied presentation and often mimics pancreatic malignancy, which can make the diagnosis challenging. Most patients have an excellent response to corticosteroid therapy. Immunomodulators may be used in some cases. Rituximab is an effective, emerging treatment in steroid‐refractory cases.… Show more

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Cited by 9 publications
(10 citation statements)
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“…In conclusion, our study is the first to summarize the differences in clinical phenotypes among Chinese and Western AIP populations. The reason caused the differences between the eastern and western AIP phenotype is unclear, which may include the genetic background, environmental factor, dietary factors ( 35 ). However, there are some limitations of the study that need to be considered.…”
Section: Discussionmentioning
confidence: 99%
“…In conclusion, our study is the first to summarize the differences in clinical phenotypes among Chinese and Western AIP populations. The reason caused the differences between the eastern and western AIP phenotype is unclear, which may include the genetic background, environmental factor, dietary factors ( 35 ). However, there are some limitations of the study that need to be considered.…”
Section: Discussionmentioning
confidence: 99%
“…122,123 One of the few GI disorders for which rituximab showed a favorable response, including safety and efficacy, is autoimmune pancreatitis. [124][125][126][127][128][129][130][131][132] Patients afflicted with this disease experience remission, and consequently, relief from severe abdominal pain after rituximab treatment. Overall, rituximab provided clinical benefit in 22%…”
Section: Gastroenterologymentioning
confidence: 99%
“… 1 Type 1 AIP predominantly affects male adults and has multiorgan extrapancreatic manifestations (ie, sclerosing cholangitis, interstitial nephritis, sclerosing sialadenitis, mediastinal fibrosis, and thyroiditis). 2 However, it is much less associated with inflammatory bowel disease compared with type 2 AIP, which is reported to have a least 15% predilection for ulcerative colitis. 2 It is believed that the cause of AIP maybe multifactorial from immunological, genetic, and/or environmental and that an inciting event in genetically predisposed individuals may trigger AIP.…”
Section: Introductionmentioning
confidence: 99%
“… 2 However, it is much less associated with inflammatory bowel disease compared with type 2 AIP, which is reported to have a least 15% predilection for ulcerative colitis. 2 It is believed that the cause of AIP maybe multifactorial from immunological, genetic, and/or environmental and that an inciting event in genetically predisposed individuals may trigger AIP. To date, there are no reports of vaccine-induced type 1 AIP.…”
Section: Introductionmentioning
confidence: 99%