Autoimmune pancreatitis (AIP) is a distinct form of chronic pancreatitis that typically presents with obstructive jaundice, abdominal discomfort, and other clinical manifestations. It is immune-mediated and marked by lymphocytic and plasmacytic infiltration, pancreatic fibrosis, pancreatic dysfunction, and possible extrapancreatic organ involvement, and it generally responds well to glucocorticoid therapy.