Article ID Journal Published Year Pages File Type
4251444 Seminars in Nuclear Medicine 2007 17 Pages PDF
Abstract

The use of 18F-fluorodeoxyglucose positron emission tomography (18F-FDG-PET) in the field of oncology is rapidly evolving; however, 18F-FDG is not tumor specific. Aside from physiological uptake 18F-FDG also may accumulate in benign processes. Knowledge of these 18F-FDG-avid nonmalignant lesions is essential for accurate PET interpretation in oncologic patients to avoid a false-positive interpretation. Through the systematic review of the reports of PET/computed tomography (CT) studies performed in oncologic patients during a 6-month period, we found benign nonphysiological uptake of 18F-FDG in more than 25% of studies. In half of these, 18F-FDG uptake was moderate or marked in intensity, similar to that of malignant sites. A total of 73% of benign lesions were inflammatory in nature, with post-traumatic bone and soft-tissue abnormalities (including iatrogenic injury) and benign tumors accounting for the remainder. The differentiation of benign from malignant uptake of 18F-FDG on PET alone may be particularly challenging as a result of the low anatomical resolution of PET and paucity of anatomical landmarks. Fusion imaging, namely PET/CT, has been shown to improve not only the sensitivity of PET interpretation but also its specificity. Aside from better anatomical localization of lesions on PET/CT, morphological characterization of lesions on CT often may improve the diagnostic accuracy of nonspecific 18F-FDG uptake. Correlation with CT on fused PET/CT data may obviate the need for further evaluation or biopsy in more than one-third of scintigraphic equivocal lesions. Familiarity with 18F-FDG-avid nonmalignant lesions also may extend the use of 18F-FDG-PET imaging beyond the field of oncology. We have tabulated our experience with benign entities associated with increased 18F-FDG uptake on whole-body PET/CT from 12,000 whole-body 18F-FDG-PET/CT studies performed during a 4-year period.

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