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- W2051275935 abstract "Autoimmune pancreatitis (AIP) is defined as a particular form of pancreatitis that often manifests as obstructive jaundice associated with a pancreatic mass or an obstructive bile duct lesion, and that has an excellent response to corticosteroid treatment. The prevalence of AIP worldwide is unknown, and it is considered as a rare entity. The clinical and radiological presentation of AIP can mimic bilio-pancreatic cancer, presenting difficulties for diagnosis and obliging the surgeon to balance decision-making between the potential risk presented by the misdiagnosis of a deadly disease against the desire to avoid unnecessary major surgery for a disease that responds effectively to corticosteroid treatment. In this review we detail the current and critical points for the diagnosis, classification and treatment for AIP, with a special emphasis on surgical series and the methods to differentiate between this pathology and bilio-pancreatic cancer." @default.
- W2051275935 created "2016-06-24" @default.
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- W2051275935 date "2014-12-01" @default.
- W2051275935 modified "2023-09-25" @default.
- W2051275935 title "Pancreatitis autoinmune: un dilema quirúrgico" @default.
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- W2051275935 doi "https://doi.org/10.1016/j.ciresp.2014.01.013" @default.
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