Steroid-resistant Relapse of Autoimmune Pancreatitis with Marked Main Pancreatic Duct Dilatation Mimicking Multifocal Pancreatic Cancer

Read full text
Authors: Kenji Hirano, Kanami Kondo, Toshifumi Saito, Keigo Takahashi, Shinji Ono, Sohei Abe, Tomoji Kato, Katsuya Kobayashi, Kenichiro Sekigawa, Hiroshi Mitsui
Cited by: 1
References: 12

Abstract

A 67-year-old man with type 1 autoimmune pancreatitis (AIP) and IgG4-related sclerosing cholangitis experienced a relapse, while presenting with pancreatic head swelling and distal bile duct stenosis. Despite an increase in the prednisolone dosage (from 7.5 to 20 mg/day), the disease worsened. A significant dilatation of the main pancreatic duct (8 mm) and new stenosis of the pancreatic tail duct were observed. Malignancy was ruled out by repeated endoscopic ultrasound-guided fine-needle aspiration biopsies. A further escalation of the prednisolone dose to 40 mg/day led to clinical and radiological improvements. This case underscores the difficulty in distinguishing a steroid-resistant AIP relapse from pancreatic cancer, and the importance of ruling out malignancy before intensifying immunosuppressive therapy.

Fields of Study & Subjects

IgG4-Related and Inflammatory Diseases Liver Diseases and Immunity Pancreatitis Pathology and Treatment

Publication details

Journal / source
Internal Medicine
Publisher
Japanese Society of Internal Medicine
Volume
65
Issue
17
Pages
2317–2322
Publication date
14 January 2026
Language
EN