Clinicopathological study of surgically treated non-neoplastic diseases of the pancreas with special reference to autoimmune pancreatitis

Author:

Seki Makoto1,Ninomiya Eiji1,Saiura Akio2,Takahashi Yu1,Inoue Yosuke1,Katori Masamichi1,Yamamoto Noriko1,Takamatsu Manabu1,Kato Yo1,Yamada Keiko1,Matsueda Kiyoshi1,Ohkura Yasuo3

Affiliation:

1. Cancer Institute of the Japanese Foundation for Cancer Research

2. Juntendo University Hospital

3. Kyorin University School of Medicine

Abstract

Abstract Purpose After the popularization of serum immunoglobulin G4 (IgG4) measurement and endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) in our institute, surgical resection for non-neoplastic diseases of the pancreas became less common. Although the incidence of such false-positive cases was clarified in the 10-year period after introduction of these measures (2009–2018), these data were not compared with the 30 years before 2009 (1979–2008). This study was performed to determine the percentage of autoimmune pancreatitis (AIP) that was included during the latter period and how the numbers of false-positive cases differed between the two periods. Methods From 1979 to 2008, 51 patients had clinical suspicion of pancreatic carcinoma (false-positive disease). Among these 51 patients, 32 non-alcoholic patients who had tumor-forming chronic pancreatitis (TFCP) were clinically, histologically, and immunohistochemically compared with 11 patients who had TFCP during the latter 10-year period. Results Retrospective IgG4 immunostaining of TFCP revealed 14 (43.8%) cases of AIP in the former 30 years versus 5 (45.5%) in the latter 10 years. There were 32 (6.7%) cases of TFCP among 675 patients in the former 30 years and 11 (0.9%) among 1289 patients in the latter 10 years. Conclusions When the TFCP ratio of pancreatic resections and the AIP ratio of TFCPs were compared between the two periods, the TFCP ratio was 4.7% versus 0.9% and the AIP ratio was 43.8% versus 45.5%, respectively. These findings indicate that IgG4 measurement and EUS-FNA are imperative for the diagnosis of TFCP.

Publisher

Research Square Platform LLC

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