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Multifocal lesions with pancreatic atrophy in IgG4-related autoimmune pancreatitis: report of a case
Authors:Akifumi Kimura  Junji Yamamoto  Kazuo Hatsuse  Suefumi Aosasa  Kiyoshi Nishiyama  Tadashi Maejima  Sho Ogata  Hideyuki Shimazaki  Atsushi Kawaguchi  Kazuo Hase
Affiliation:1. Department of Surgery, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan
2. Department of Pathology and Laboratory Medicine, National Defense Medical College, Tokorozawa, Japan
3. Department of Laboratory Medicine, National Defense Medical College Hospital, Tokorozawa, Japan
4. Department of Internal Medicine, National Defense Medical College, Tokorozawa, Japan
Abstract:
We herein report a case of IgG4-related autoimmune pancreatitis (AIP). A 72-year-old male with jaundice visited our hospital complaining of epigastralgia. A blood chemistry analysis revealed elevated serum levels of total bilirubin and DUPAN-II. Computed tomography (CT) revealed irregularly shaped pancreatic masses with a stricture of the main pancreatic duct (MPD) in the head and tail that were interposed by marked atrophy with MPD dilation in the body. F-18 fluorodeoxyglucose (FDG)-positron emission tomography/CT revealed abnormally intense FDG uptake only at the masses. During surgery, another small tumor was also found in the atrophied body; therefore, a total pancreatectomy was performed under the diagnosis of multiple pancreatic cancers. The histological analysis revealed fibrosis with dense and diffuse infiltrations of lymphocytes and IgG4-positive plasma cells. The pancreatic parenchyma of the body was firmly replaced by fibrosis. AIP can lead to the formation of multiple pancreatic lesions, and thus the correct diagnosis is occasionally difficult to establish in atypical cases.
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