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. 2014 Nov 14;20(42):15580–15589. doi: 10.3748/wjg.v20.i42.15580

Table 2.

Position emission tomography/computed tomography in differential diagnosis of pancreatic carcinoma and mass-forming pancreatitis

Ref.1 Study design PC/CP SUV(max) of PC SUV(max) of CP Cutoff value SE SP PPV NPV LR(+) LR(-) Accuracy
(mean ± SD) (mean ± SD)
Stollfuss et al[25] R 43/30 3.16 ± 1.22 1.00 ± 0.55 1.53 93.18% 93.10% 95.35% 90.00% 13.51 0.07 93.15%
Mertz et al[21] R 31/4 - - 2.80 87.09% 50.00% 93.33% 33.33% 1.74 0.25 82.86%
van Kouwen et al[19] R 32/77 - - -2 90.62% 87.01% 74.35% 95.71% 6.97 0.11 88.07%
Lytras et al[18] R 54/25 - - -3 78.00% 55.00% 78.00% 55.00% - - 64.00%
1

Fluorodeoxyglucose-position emission tomography (FDG-PET) scan without computed tomography (CT);

2

Results were judged to be abnormal if focal accumulation of the tracer was detected in the area of the pancreas. Faint and/or diffuse FDG uptake in the pancreatic region (i.e., uptake slightly higher than the surrounding background, but clearly lower than the liver) was not considered suspicious for pancreatic cancer;

3

Lesions measured visually. SE: Sensitivity; SP: Specificity; NPV: Negative predictive value; PPV: Positive predictive value; R: Retrospective study; P: Prospective study.