The efficacy of whole-body FDG-PET or PET/CT for autoimmune pancreatitis and associated extrapancreatic autoimmune lesions

• Published in: European journal of nuclear medicine and molecular imaging 2007-12, Vol.34 (12), p.2088-2095
• Main Authors: Nakajo, Masatoyo, Jinnouchi, Seishi, Fukukura, Yoshihiko, Tanabe, Hiroaki, Tateno, Rie, Nakajo, Masayuki
• Format: Article
• Language: English
• Subjects: Aged; Autoimmune diseases; Autoimmune Diseases - diagnosis; Female; Fluorodeoxyglucose F18; Humans; Male; Medical imaging; Middle Aged; Nuclear medicine; Pancreas; Pancreatitis - diagnosis; Positron-Emission Tomography - methods; Radiopharmaceuticals; Reproducibility of Results; Sensitivity and Specificity; Subtraction Technique; Tomography; Tomography, X-Ray Computed - methods; Whole Body Imaging - methods
• ISSN: 1619-7070; 1619-7089
• DOI: 10.1007/s00259-007-0562-7

The aim of this study was to evaluate retrospectively the efficacy of whole-body (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) for autoimmune pancreatitis (AIP) and associated extrapancreatic autoimmune lesions. Whole-body FDG-PET or PET/computed tomography (CT) findings were reviewed in six patients with AIP. The initial PET scans were performed 1 h and 2 h after FDG injection in all six patients. Follow-up PET scans were performed during or following steroid therapy in five patients and in one patient who did not have steroid therapy. The initial PET scans revealed intense FDG uptake by AIP in all six patients. The maximum standardized uptake value (SUVmax) increased in four patients and was stable in two patients. The intense uptake in the pancreas disappeared during or following steroid therapy in five patients and in one patient who showed spontaneous remission of AIP. Abnormal FDG uptake by extrapancreatic autoimmune diseases was observed in five of the six patients: sclerosing sialadenitis (n = 5), lymphadenopathy (n = 5), retroperitoneal fibrosis (n = 2), interstitial nephritis (n = 2) and sclerosing cholecystitis (n = 1). Abnormal FDG uptake disappeared in the salivary glands (n = 4), lymph nodes (n = 4), retroperitoneum (n = 2), kidneys (n = 1) and gallbladder (n = 1) during or following steroid therapy and remained in the salivary glands and lymph nodes of a spontaneous remission patient. These results suggest that whole-body FDG-PET may be useful for detecting AIP and associated extrapancreatic autoimmune lesions and for monitoring their disease activity but that dual time point imaging may not be useful for differentiating malignancy from AIP.