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World J Gastroenterol. Jan 28, 2008; 14(4): 601-606
Published online Jan 28, 2008. doi: 10.3748/wjg.14.601
Diagnosis and management of autoimmune pancreatitis: Experience from China
Yang Song, Quan-Da Liu, Ning-Xin Zhou, Wen-Zhi Zhang, Dian-Jun Wang
Yang Song, Emergency Department, Chinese PLA General Hospital, 28th Fuxing Road, Beijing 100853 China
Quan-Da Liu, Ning-Xin Zhou, Wen-Zhi Zhang, Institute of Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China
Dian-Jun Wang, Department of Pathology, Chinese PLA General Hospital, Beijing 100853, China
Correspondence to: Quan-Da Liu, MD, PhD, Institute of Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China. liuquanda@sina.com
Telephone: +86-13911088630
Fax: +86-10-68183622
Received: October 20, 2007
Revised: November 16, 2007
Published online: January 28, 2008
Abstract

AIM: To determine the clinical, radiographic and pathologic characteristics, diagnostic and treatment modalities in patients with autoimmune pancreatitis (AIP).

METHODS: In this retrospective study, the data of patients with diagnosed chronic pancreatitis (CP) between 1995 and 2006 in Chinese PLA General Hospital were included to screen for the cases with AIP, according to the following diagnostic criteria: (1) diagnostic histopathologic features, and abound IgG4-positive plasma cells on pancreatic tissues; (2) characteristic imaging on computed tomography and pancreatography, together with increased serum IgG, γ-globulin levels or presence of autoantibodies; (3) response to steroid therapy. The clinical, radiographic and pathologic characteristics, diagnostic and treatment modalities, and outcome of AIP cases were reviewed.

RESULTS: Twenty-five (22 male, 3 female; mean age 54 years, 36-76 years) out of 510 CP patients were diagnosed as AIP, which accounted for 49% (21/43) of CP population undergoing surgical treatment in the same period. The main clinical manifestations included intermittent or progressive jaundice in 18 cases (72%), abdominal pain in 11 (44%), weight loss in 10 (40%), and 3 cases had no symptoms. The imaging features consisted of pancreatic enlargement, especially in the head of pancreas (18 cases), strictures of main pancreatic duct and intrapancreatic bile duct. Massive lymphocytes and plasma cells infiltration in pancreatic tissues were showed on pathology, as well as parenchymal fibrosis. Twenty-three patients were misdiagnosed as pancreaticobiliary malignancy, and 21 patients underwent exploratory laparotomy, the remaining 4 patients dramatically responded to steroid therapy. No pancreatic cancer occurred during a mean 46-mo follow-up period.

CONCLUSION: AIP patients always are subjected to mistaken diagnosis of pancreatic cancer and an unnecessary surgical exploration, due to its similarity in clinical features with pancreatic cancer. The differential diagnosis with high index of suspicion of AIP would improve the diagnostic accuracy for AIP.

Keywords: Autoimmune pancreatitis; Pancreatic neoplasms; Differential diagnosis; Steroid therapy