Metser Ur, Even-Sapir Einat
Department of Nuclear Medicine, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
Semin Nucl Med. 2007 May;37(3):206-22. doi: 10.1053/j.semnuclmed.2007.01.001.
The use of (18)F-fluorodeoxyglucose positron emission tomography ((18)F-FDG-PET) in the field of oncology is rapidly evolving; however, (18)F-FDG is not tumor specific. Aside from physiological uptake (18)F-FDG also may accumulate in benign processes. Knowledge of these (18)F-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 (18)F-FDG in more than 25% of studies. In half of these, (18)F-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 (18)F-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 (18)F-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 (18)F-FDG-avid nonmalignant lesions also may extend the use of (18)F-FDG-PET imaging beyond the field of oncology. We have tabulated our experience with benign entities associated with increased (18)F-FDG uptake on whole-body PET/CT from 12,000 whole-body (18)F-FDG-PET/CT studies performed during a 4-year period.
(18)F-氟脱氧葡萄糖正电子发射断层扫描((18)F-FDG-PET)在肿瘤学领域的应用正在迅速发展;然而,(18)F-FDG并非肿瘤特异性的。除了生理性摄取外,(18)F-FDG也可能在良性病变中蓄积。了解这些摄取(18)F-FDG的非恶性病变对于准确解读肿瘤患者的PET检查结果以避免假阳性解读至关重要。通过系统回顾在6个月期间对肿瘤患者进行的PET/计算机断层扫描(CT)研究报告,我们发现在超过25%的研究中存在(18)F-FDG的良性非生理性摄取。其中一半的研究中,(18)F-FDG摄取强度为中度或明显,与恶性部位相似。总共73%的良性病变本质上是炎症性的,其余为创伤后骨和软组织异常(包括医源性损伤)以及良性肿瘤。由于PET的解剖分辨率低且解剖标志少,仅通过PET区分(18)F-FDG的良性与恶性摄取可能特别具有挑战性。融合成像,即PET/CT,已被证明不仅能提高PET解读的敏感性,还能提高其特异性。除了在PET/CT上对病变进行更好的解剖定位外,CT上病变的形态学特征通常也可提高对非特异性(18)F-FDG摄取的诊断准确性。在超过三分之一的闪烁显像结果不明确的病变中,将PET/CT融合数据与CT相关联可能无需进一步评估或活检。熟悉摄取(18)F-FDG的非恶性病变还可能将(18)F-FDG-PET成像的应用扩展到肿瘤学领域之外。我们汇总了在4年期间进行的12000例全身(18)F-FDG-PET/CT研究中,与全身PET/CT上(18)F-FDG摄取增加相关的良性病变的经验。