18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancer

Abstract Background 18F-FDG PET/CT could satisfactorily show pancreatic and extra-pancreatic lesions in AIP, which can be mistaken for pancreatic cancer (PC). This study aimed to identify 18F-FDG PET/CT findings that might differentiate AIP from PC. Methods FDG-PET/CT findings of 26 AIP and 40 PC pa...

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Main Authors: Jian Zhang, Guorong Jia, Changjing Zuo, Ningyang Jia, Hui Wang
Format: Article
Language:English
Published: BMC 2017-10-01
Series:BMC Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12885-017-3665-y
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author Jian Zhang
Guorong Jia
Changjing Zuo
Ningyang Jia
Hui Wang
author_facet Jian Zhang
Guorong Jia
Changjing Zuo
Ningyang Jia
Hui Wang
author_sort Jian Zhang
collection DOAJ
description Abstract Background 18F-FDG PET/CT could satisfactorily show pancreatic and extra-pancreatic lesions in AIP, which can be mistaken for pancreatic cancer (PC). This study aimed to identify 18F-FDG PET/CT findings that might differentiate AIP from PC. Methods FDG-PET/CT findings of 26 AIP and 40 PC patients were reviewed. Pancreatic and extra-pancreatic lesions related findings, including maximum standardized uptake values (SUVmax) and patterns of FDG uptake, were identified and compared. Results All 26 patients with AIP had increased pancreatic FDG uptake. Focal abnormal pancreatic FDG activities were found in 38/40 (95.00%) PC patients, while longitudinal were found in 18/26 (69.23%) AIP patients. SUVmax was significantly different between AIP and PC, both in early and delayed PET/CT scans (p < 0.05). AUCs were 0.700 (early SUVmax), 0.687 (delayed SUVmax), 0.683 (early lesions/liver SUVmax), and 0.715 (delayed lesion/liver SUVmax). Bile duct related abnormalities were found in 12/26 (46.15%) AIP and 10/40 (25.00%) PC patients, respectively. Incidentally, salivary and prostate gland SUVmax in AIP patients were higher compared with those of PC patients (p < 0.05). In males,an inverted “V” shaped high FDG uptake in the prostate was more frequent in AIP than PC patients (56.00%, 14/25 vs. 5.71%, 2/35). Increased FDG activity in extra-pancreatic bile duct was present in 4/26 of AIP patients, while was observed in none of the PC patients. Only in AIP patients, both diffuse pancreatic FDG accumulation and increased inverted “V” shaped FDG uptake in the prostate could be found simultaneously. Conclusions 18F-FDG PET/CT findings might help differentiate AIP from PC.
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spelling doaj.art-d4159abcfc19447b882ae01db2826f0b2022-12-22T01:55:07ZengBMCBMC Cancer1471-24072017-10-011711910.1186/s12885-017-3665-y18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancerJian Zhang0Guorong Jia1Changjing Zuo2Ningyang Jia3Hui Wang4Department of Nuclear Medicine, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of MedicineDepartment of Nuclear Medicine, Changhai Hospital, Second Military Medical UniversityDepartment of Nuclear Medicine, Changhai Hospital, Second Military Medical UniversityDepartment of Radiology, Eastern Hepatobiliary Surgery Hospital, Second Military Medical UniversityDepartment of Nuclear Medicine, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of MedicineAbstract Background 18F-FDG PET/CT could satisfactorily show pancreatic and extra-pancreatic lesions in AIP, which can be mistaken for pancreatic cancer (PC). This study aimed to identify 18F-FDG PET/CT findings that might differentiate AIP from PC. Methods FDG-PET/CT findings of 26 AIP and 40 PC patients were reviewed. Pancreatic and extra-pancreatic lesions related findings, including maximum standardized uptake values (SUVmax) and patterns of FDG uptake, were identified and compared. Results All 26 patients with AIP had increased pancreatic FDG uptake. Focal abnormal pancreatic FDG activities were found in 38/40 (95.00%) PC patients, while longitudinal were found in 18/26 (69.23%) AIP patients. SUVmax was significantly different between AIP and PC, both in early and delayed PET/CT scans (p < 0.05). AUCs were 0.700 (early SUVmax), 0.687 (delayed SUVmax), 0.683 (early lesions/liver SUVmax), and 0.715 (delayed lesion/liver SUVmax). Bile duct related abnormalities were found in 12/26 (46.15%) AIP and 10/40 (25.00%) PC patients, respectively. Incidentally, salivary and prostate gland SUVmax in AIP patients were higher compared with those of PC patients (p < 0.05). In males,an inverted “V” shaped high FDG uptake in the prostate was more frequent in AIP than PC patients (56.00%, 14/25 vs. 5.71%, 2/35). Increased FDG activity in extra-pancreatic bile duct was present in 4/26 of AIP patients, while was observed in none of the PC patients. Only in AIP patients, both diffuse pancreatic FDG accumulation and increased inverted “V” shaped FDG uptake in the prostate could be found simultaneously. Conclusions 18F-FDG PET/CT findings might help differentiate AIP from PC.http://link.springer.com/article/10.1186/s12885-017-3665-yAutoimmune pancreatitisPancreatic cancerPositron-emission tomography
spellingShingle Jian Zhang
Guorong Jia
Changjing Zuo
Ningyang Jia
Hui Wang
18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancer
BMC Cancer
Autoimmune pancreatitis
Pancreatic cancer
Positron-emission tomography
title 18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancer
title_full 18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancer
title_fullStr 18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancer
title_full_unstemmed 18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancer
title_short 18F- FDG PET/CT helps differentiate autoimmune pancreatitis from pancreatic cancer
title_sort 18f fdg pet ct helps differentiate autoimmune pancreatitis from pancreatic cancer
topic Autoimmune pancreatitis
Pancreatic cancer
Positron-emission tomography
url http://link.springer.com/article/10.1186/s12885-017-3665-y
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AT changjingzuo 18ffdgpetcthelpsdifferentiateautoimmunepancreatitisfrompancreaticcancer
AT ningyangjia 18ffdgpetcthelpsdifferentiateautoimmunepancreatitisfrompancreaticcancer
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