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World J Gastroenterol. Dec 7, 2014; 20(45): 16881-16890
Published online Dec 7, 2014. doi: 10.3748/wjg.v20.i45.16881
Autoimmune pancreatitis: Multimodality non-invasive imaging diagnosis
Stefano Crosara, Mirko D'Onofrio, Riccardo De Robertis, Emanuele Demozzi, Stefano Canestrini, Giulia Zamboni, Roberto Pozzi Mucelli
Stefano Crosara, Riccardo De Robertis, Emanuele Demozzi, Stefano Canestrini, Giulia Zamboni, Roberto Pozzi Mucelli, Mirko D’Onofrio, Department of Radiology, University Hospital GB Rossi, University of Verona, 37134 Verona, Italy
Author contributions: All the authors equally contributed to this paper.
Correspondence to: Mirko D’Onofrio, MD, Assistant Professor, Department of Radiology, University Hospital GB Rossi, University of Verona, Piazzale LA Scuro 10, 37134 Verona, Italy. mirko.donofrio@univr.it
Telephone: +39-45-8124140 Fax: +39-45-8277808
Received: April 23, 2014
Revised: July 3, 2014
Accepted: September 12, 2014
Published online: December 7, 2014
Processing time: 225 Days and 11 Hours
Abstract

Autoimmune pancreatitis (AIP) is characterized by obstructive jaundice, a dramatic clinical response to steroids and pathologically by a lymphoplasmacytic infiltrate, with or without a pancreatic mass. Type 1 AIP is the pancreatic manifestation of an IgG4-related systemic disease and is characterized by elevated IgG4 serum levels, infiltration of IgG4-positive plasma cells and extrapancreatic lesions. Type 2 AIP usually has none or very few IgG4-positive plasma cells, no serum IgG4 elevation and appears to be a pancreas-specific disorder without extrapancreatic involvement. AIP is diagnosed in approximately 2%-6% of patients that undergo pancreatic resection for suspected pancreatic cancer. There are three patterns of autoimmune pancreatitis: diffuse disease is the most common type, with a diffuse, “sausage-like” pancreatic enlargement with sharp margins and loss of the lobular contours; focal disease is less common and manifests as a focal mass, often within the pancreatic head, mimicking a pancreatic malignancy. Multifocal involvement can also occur. In this paper we describe the features of AIP at ultrasonography, computed tomography, magnetic resonance and positron emission tomography/computed tomography imaging, focusing on diagnosis and differential diagnosis with pancreatic ductal adenocarcinoma. It is of utmost importance to make an early correct differential diagnosis between these two diseases in order to identify the optimal therapeutic strategy and to avoid unnecessary laparotomy or pancreatic resection in AIP patients. Non-invasive imaging plays also an important role in therapy monitoring, in follow-up and in early identification of disease recurrence.

Keywords: Autoimmune pancreatitis; Pancreatic imaging; Ultrasonography; Computed tomography; Magnetic resonance

Core tip: In this paper we describe the features of autoimmune pancreatitis (AIP) at ultrasonography, computed tomography, magnetic resonance and positron emission tomography/computed tomography imaging, focusing on diagnosis and differential diagnosis with pancreatic ductal adenocarcinoma, which has a similar imaging appearance but a completely different therapeutic management. It is of utmost importance to make an early correct differential diagnosis between these two diseases in order to identify the optimal therapeutic strategy and to avoid unnecessary laparotomy or pancreatic resection in AIP patients. Non-invasive imaging plays also an important role in therapy monitoring, in follow-up and in early identification of disease recurrence.