MR Spectroscopy for Differentiating Benign From Malignant Solid Adnexal Tumors

作者:Ma Feng Hua; Qiang Jin Wei*; Cai Song Qi; Zhao Shu Hui; Zhang Guo Fu; Rao Ya Min
来源:American Journal of Roentgenology, 2015, 204(6): W724-W730.
DOI:10.2214/AJR.14.13391

摘要

OBJECTIVE. The purpose of this article is to investigate the proton MR spectroscopy (H-1-MRS) features of solid adnexal tumors and to evaluate the efficacy of H-1-MRS for differentiating benign from malignant solid adnexal tumors. MATERIALS AND METHODS. Sixty-nine patients with surgically and histologically proven solid adnexal tumors (27 benign and 42 malignant) underwent conventional MRI and 1H-MRS. Single-voxel spectroscopy was performed using the point-resolved spectroscopy localization technique with a voxel size of 2 x 2 x 2 cm(3). Resonance peak integrals of choline, N-acetyl aspartate (NAA), creatine, lactate, and lipid were analyzed, and the choline-to-creatine, NAA-to-creatine, lactate-to-creatine, and lipid-to-creatine ratios were recorded and compared between benign and malignant tumors. RESULTS. A choline peak was detected in all 69 cases (100%), NAA peak in 67 cases (97%, 25 benign and 42 malignant), lipid peak in 47 cases (17 benign and 30 malignant), and lactate peak in eight cases (four benign and four malignant). The mean (+/- SD) choline-to-creatine ratio was 5.13 +/- 0.6 in benign tumors versus 8.90 +/- 0.5 in malignant solid adnexal tumors, a statistically significant difference (p = 0.000). There were no statistically significant differences between benign and malignant tumors in the NAA-to-creatine and lipid-to-creatine ratios (p = 0.263 and 0.120, respectively). When the choline-to-creatine threshold was 7.46 for differentiating between benign and malignant tumors, the sensitivity, specificity, and accuracy were 94.1%, 97.1%, and 91.2%, respectively. CONCLUSION. Our preliminary study shows that the H-1-MRS patterns of benign and malignant solid adnexal tumors differ. The choline-to-creatine ratio can help clinicians differentiate benign from malignant tumors.