Purpose: F-18 fluorodeoxyglucose (FDG) may accumulate at sites of inflammat
ion or infection, making interpretation of whole-body scans difficult in pa
tients with cancer.
Methods: More than 650 whole-body positron emission tomographic (PET) scans
performed to examine patients with cancer were reviewed to identify uptake
in pulmonary infection or inflammation based on the appearance of F-18 FDG
chest uptake, chest radiographs, computed tomography, or all of these.
Results: Ten patients had uptake in benign lung disease. Eight patients had
head and neck tumors and two patients had breast cancer. Intense focal or
multifocal F-18 FDG chest uptake was seen in 6 of 10 scans. This was diffic
ult to distinguish from pulmonary metastases based on the scan appearance.
However, in the remaining patients, the uptake was atypical for malignancy
and displayed an apical, segmental, or lobar pattern. In all patients, the
F-18 FDG lung uptake corresponded to benign radiologic changes (infiltratio
n, consolidation, or atelectasis), and the final diagnosis was pulmonary in
flammation or infection. Nine patients were asymptomatic and one patient ha
d clinical aspiration pneumonia. Follow-up PET scans were performed in five
patients to evaluate their conditions. Chest uptake disappeared completely
in three patients and partially in two patients, and there were no new fin
dings. Variable degrees of F-18 FDG chest uptake have been reported with mo
re than 40 different benign causes. They can be classified based on the und
erlying mechanism into four major categories: 1) Inflammation or infection,
2) benign tumor, 3) physiologic activity, and 4) iatrogenic. Most of these
false-positive cases are included in the first category.
Conclusions: Pulmonary infection or inflammation might predispose patients
to localized F-18 FDG chest uptake mimicking pulmonary metastases and limit
ing the specificity of whole-body scans performed in patients with cancer.