Journal of Clinical Medicine, Journal Year: 2025, Volume and Issue: 14(9), P. 3076 - 3076

Published: April 29, 2025

Autoimmune pancreatitis is a rare condition of pancreatic inflammation with two classic subtypes. The emergence third subtype, ICI-induced pancreatitis, highlights the need for knowledge each type to ensure accurate diagnosis and treatment. Abbreviations: AIP—Autoimmune pancreatitis; AIP-1—Type 1 autoimmune also known as lymphoplasmacytic sclerosing (LPSP); AIP-2—Type 2 referred idiopathic duct-centric (IDCP); AIP-3—Type 3 immune checkpoint inhibitor (ICI)-induced IgG4-RD—Immunoglobulin G4-related disease.

Language: Английский