Utility of 18F‐fluorodeoxyglucose‐positron emission tomography in the differential diagnosis of benign and malignant gynaecological tumours
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18F-FDG PET/CT's SUVmax effectively differentiates benign from malignant ovarian and uterine tumours, showing higher uptake in malignant masses.
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Abstract
INTRODUCTION: Positron emission tomography/computed tomography (PET/CT) involving 18F-fluorodeoxyglucose (FDG) is widely used for systemic cancer and recurrence diagnosis. However, the differential diagnosis of benign and malignant gynaecological tumours according to FDG accumulation is unclear. This study aimed to investigate the intensity of FDG uptake/metabolic activity for the differential diagnosis of benign and malignant gynaecological tumours. METHODS: This study included seven patients with physiological phenomena, 34 with benign tumours, 13 with borderline malignant tumours and 119 with malignant tumours who underwent 18F-FDG PET/CT. We assessed the maximum standardized uptake value (SUVmax) and determined its utility in the diagnosis of benign and malignant tumours using a receiver operating characteristic (ROC) curve analysis. RESULTS: Among the 63 patients with ovarian tumours, the mean SUVmax of 22 patients with benign ovarian tumours was 2.48 and the mean SUVmax of 41 patients with malignant ovarian tumours was 10.98 (P < 0.001). In the ROC curve analysis, the area under the curve (AUC) was 0.977, with a 95% confidence interval of 0.947-1.000. With a cut-off value of 3.97 for the optimal SUVmax, the sensitivity and specificity were 95.1% and 86.4%, respectively. In addition, the AUC was 0.911 (95% CI: 0.768-1.000) for the assessment of uterine myomas and sarcomas. With a cut-off value of 10.62 for the optimal SUVmax, the sensitivity and specificity were 91.7% and 86.7% respectively. CONCLUSIONS: The SUVmax value helps differentiate benign and malignant ovarian tumours, as well as uterine myomas and uterine sarcomas.
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References (29)
- doi:10.1002/1097-0142(19901015)60:8+<2035::aid-cncr2820601515>3.0.co;2-8 via openalex
- doi:10.1097/01.grf.0000159538.27221.8c via openalex
- doi:10.1097/mnm.0b013e328345b339 via openalex
- doi:10.1159/000294861 via openalex
- doi:10.1016/s0020-7292(12)60024-1 via openalex
- doi:10.1038/nrc882 via openalex
- W1923700521 via openalex
- doi:10.1097/01.aog.0000136079.62513.39 via openalex
- doi:10.1097/00004347-199304000-00006 via openalex
- doi:10.1007/s12149-008-0227-z via openalex
- doi:10.1097/00006231-200409000-00012 via openalex
- doi:10.1002/uog.5365 via openalex
- W2119602980 via openalex
- doi:10.2214/ajr.09.4074 via openalex
- W2418330216 via openalex
- W2762390991 via openalex
- W6640204121 via openalex
- W6745205409 via openalex
- doi:10.1016/j.ijgo.2008.12.008 via openalex
- doi:10.1007/bf01542654 via openalex
- doi:10.1111/igc.0b013e31819a1f8f via openalex
- doi:10.1097/igc.0000000000000301 via openalex
- doi:10.1126/science.123.3191.309 via openalex
- doi:10.3802/jgo.2015.26.2.87 via openalex
- doi:10.1056/nejm198310133091503 via openalex
- doi:10.1097/igc.0000000000000074 via openalex
- doi:10.1097/mnm.0b013e32832bcaec via openalex
- doi:10.3802/jgo.2017.28.e28 via openalex
- doi:10.1007/s00259-004-1703-x via openalex
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