Characterizing IgG4-related disease with 18F-FDG PET/CT: a prospective cohort study

Jingjing Zhang(Peking Union Medical College Hospital), Hua Chen(Peking Union Medical College Hospital), Yanru Ma(Peking Union Medical College Hospital), Yu Xiao(Peking Union Medical College Hospital), Na Niu(Chinese Academy of Medical Sciences & Peking Union Medical College), Wei Lin(Peking Union Medical College Hospital), Xinwei Wang(Peking Union Medical College Hospital), Zhiyong Liang(Chinese Academy of Medical Sciences & Peking Union Medical College), Fengchun Zhang(Chinese Academy of Medical Sciences & Peking Union Medical College), Fang Li(Chinese Academy of Medical Sciences & Peking Union Medical College), Wen Zhang(Chinese Academy of Medical Sciences & Peking Union Medical College), Zhaohui Zhu(Chinese Academy of Medical Sciences & Peking Union Medical College)
European Journal of Nuclear Medicine and Molecular Imaging
April 24, 2014
Cited by 239Open Access
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Abstract

PURPOSE: IgG4-related disease (IgG4-RD) is an increasingly recognized clinicopathological disorder with immune-mediated inflammatory lesions mimicking malignancies. A cohort study was prospectively designed to investigate the value of (18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) in characterizing IgG4-RD. METHODS: Thirty-five patients diagnosed with IgG4-RD according to the consensus criteria were enrolled with informed consent. All patients underwent baseline (18)F-FDG PET/CT evaluation. Among them, 29 patients underwent a second (18)F-FDG PET/CT scan after 2 to 4 weeks of steroid-based therapy. RESULTS: All 35 patients were found with (18)F-FDG-avid hypermetabolic lesion(s); 97.1% (34/35) of these patients showed multi-organ involvement. Among the 35 patients, 71.4% (25/35) patients were found with more organ involvement on (18)F-FDG PET/CT than conventional evaluations including physical examination, ultrasonography, and computed tomography (CT). (18)F-FDG PET/CT demonstrated specific image characteristics and pattern of IgG4-RD, including diffusely elevated (18)F-FDG uptake in the pancreas and salivary glands, patchy lesions in the retroperitoneal region and vascular wall, and multi-organ involvement that cannot be interpreted as metastasis. Comprehensive understanding of all involvement aided the biopsy-site selection in seven patients and the recanalization of ureteral obstruction in five patients. After 2 to 4 weeks of steroid-based therapy at 40 mg to 50 mg prednisone per day, 72.4% (21/29) of the patients showed complete remission, whereas the others exhibited > 81.8% decrease in (18)F-FDG uptake. CONCLUSION: F-FDG PET/CT is a useful tool for assessing organ involvement, monitoring therapeutic response, and guiding interventional treatment of IgG4-RD. The image pattern is suggested to be updated into the consensus diagnostic criteria for IgG4-RD.


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