| Literature DB >> 29255773 |
Cláudio Martins1, Paula Lago2, Paula Sousa3, Tarcísio Araújo2, José Davide4,5, Fernando Castro-Poças2,4,5, Isabel Pedroto2,5.
Abstract
INTRODUCTION: Autoimmune pancreatitis is a rare entity of unknown etiology that can mimic pancreatic cancer and whose diagnosis involves clinical, serological, imagiological, and histological findings. There are two types of autoimmune pancreatitis: type 1, in which the pancreas is involved as one part of a systemic immunoglobulin G4-related disease, and type 2, generally without immunoglobulin G4-positive cells and without systemic involvement. CASE: We report the case of a 45-year-old female, who underwent an abdominal magnetic resonance imaging for etiological study of a solid liver lesion, which revealed a tail pancreatic mass. Laboratory analyses showed normal levels of immunoglobulin G4 and negative antinuclear antibodies. Endoscopic ultrasound revealed a homogeneous and hypoechogenic lesion in the pancreatic tail with a "sausage-like" appearance. Endoscopic ultrasound-guided fine needle aspiration was inconclusive and the patient underwent a laparoscopic distal pancreatectomy. Histopathology examination confirmed the diagnosis of type 2 autoimmune pancreatitis.Entities:
Keywords: Autoimmune pancreatitis; Immunoglobulin G4; Pancreatic cancer
Year: 2017 PMID: 29255773 PMCID: PMC5731154 DOI: 10.1159/000461589
Source DB: PubMed Journal: GE Port J Gastroenterol ISSN: 2387-1954