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Autoimmune pancreatitis type 1

rare

Type 1 autoimmune pancreatitis is a form of autoimmune pancreatitis seen in elderly males (>60 years) and presenting with abdominal pain, steatorrhea, obstructive jaundice and other organ (bile duct, kidneys and retroperitoneum) involvement. It is thought to be due to an immunoglobulin G4 (IgG4)-associated systemic disease.

Also known as
AIP type 1 · IgG4-related pancreatitis · lymphoplasmacytic sclerosing pancreatitis

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