Autoimmune pancreatitis
Autoimmune pancreatitis
Definition
Autoimmune pancreatitis (AIP) is a rare pancreatic disease characterized by chronic non-alcoholic pancreatitis that presents with abdominal pain, steatorrhea, obstructive jaundice and responds well to steroid therapy and is seen in two subforms: type 1 AIP which affects elderly males, involves other organs and has increased immunoglobin G4 (IgG4) levels and type 2 AIP which affects both sexes equally but presents at a younger age and has no other organ involvement or increased IgG4 levels.
Also known as AIP — per MONDO
Also identified as
- DOID 0040091 per MONDO
- MESH D000081012 per MONDO
- Orphanet 103919 per MONDO
- SCTID 448542008 per MONDO
- UMLS C2609129 per MONDO