Autoimmune Pancreatitis

Autoimmune pancreatitis (AIP) is a rare type of pancreatic inflammation caused by the immune system mistakenly attacking the pancreas. It can lead to abdominal pain, jaundice, and other symptoms. AIP is divided into two types, with type 1 being the most common and associated with high levels of a specific antibody. This condition responds well to corticosteroid therapy, and early detection is important for effective treatment.