Magnetic resonance imaging in the differential diagnosis of ovarian masses: Capabilities of quantitative multiparametric evaluation


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Objective. To estimate the capabilities of comprehensive magnetic resonance imaging (MRI) in the differential diagnosis of ovarian tumors. Subjects and methods. In 2011 to 2015, a total of 256patients with 289 ovarian masses underwent small pelvic and abdominal MRI (if necessary) to clarify the pattern and extent of the tumor process. MRI was performed on a 1.5 Tl scanner. The MRI protocol was to obtain T2-weighted images (WI) in three projections, STIR, T1-WI, DWI with b-factors 0, 1000м/мм2, to calculate the values of the diffusion coefficient, and to make the diffusion maps Dynamic 3D FatSat. Postprocessing involved an analysis of signal intensity-time curves in a given area of interest (8-45 pixels). MRI findings were compared with intraoperative tumor histological structural data or verified during a follow-up for at least 6 months. Results. The pattern of detected abnormalities was as follows: true ovarian tumors (71%), endometriomas (16%), cysts (11%), and tubo-ovarian abscesses (2%). Among the true tumors, there were serous epithelial tumors (51%), mucinous epithelial tumors (26%), endometrioid cysts (2%), dermoid cysts (6%), clear-cell carcinomas (2%), granulosa cell tumors (6%), fibromas (4%), Brenner tumors (1%), and metastatic tumors (3%). The degree distribution of the tumors identified was the following: benign tumors (49%), borderline tumors (12%) (occurring only in a group of epithelial tumors), and malignant tumors (39%). FIGO staging of the borderline ovarian tumors classified as Stages IA (66%) and IC (34%). That of the malignant tumors classified as Stages IA (7.3%), IIA (17%), IIB(12.2%), IIC(17%), IIIB (21.9%), IIIC(14.6%), and IV(9.7%). Quantitative estimation of the parameters of perfusion images showed that the amplitude of contrast agent accumulation was significantly higher in malignant tumors (167% (115.2-212.5%)) than in benign tumors (61.2% (41.2-99.0%)) (P < 0.001) and borderline ones (85.7% (58.3-138.2%)), (P < 0.01); the signal intensity semi-elevation period was significantly longer in benign tumors (35.1 sec (30.8-42.5sec)) than in borderline tumors (27.9sec (23.5-29.8 sec) (P < 0.05), and malignant ones (23.1 sec (20.5-30.9 sec)) (P = 0.01). The largest curvature (inflection) of the curve (%/sec) amounted to 1.78 (1.0-2.6); 2.86 (2.01-3.95), and 6.1 (4.19-9.46) for benign, borderline, and malignant tumors, respectively, and it was significantly higher in invasive carcinomas (P < 0.01). Malignant tumors have significantly lower mean apparent diffusion coefficients (ADC) than benign tumors (1.012±0.18 and 1.54±0.25 mm2/sec x 10-3, respectively); the value intervals did not intersect. The threshold ADC value of malignant ovarian tumors was lower than 1.139 mm2/sec x 10-3. The information values of advanced MRI techniques were an accuracy of 92.1%, a sensitivity of 93.6%, and a specificity of 91.2%. Conclusion. The incorporation of MRI with quantitative evaluation of perfusion parameters and diffusion-weighted images in a comprehensive examination algorithm allows differentiation of the degree of malignancy of ovarian tumors with a high degree of accuracy, by determining the opportunities for optimizing management tactics for patients.

Full Text

Restricted Access

About the authors

Alina Evgen’evna Solopova

I.M. Sechenov First Moscow State Medical University

Email: dr.solopova@mail.ru
Candidate of Medicine, assistant professor, Department of radiology and radiotherapy, Faculty of Medicine

Aleksandr Davidovich Makatsaria

I.M. Sechenov First Moscow State Medical University

Doctor of Medicine, Professor, Head of Department of Obstetrics and Gynecology, Faculty of Preventive Medicine

Aleksandr M. Sdvizhkov

GBUZ Cancer Clinic № 1 of Moscow Health Department

chief physician of clinical

Sergey Konstantinovich Ternovoy

I.M. Sechenov First Moscow State Medical University

Doctor of Medicine, Professor, Head of Department of radiology and radiotherapy, Faculty of Medicine

References

  1. Каприн А.Д., Старинский В.В., Петрова Г.В., ред. Злокачественные новообразования в России в 2013г (заболеваемость и смертность). М.: МНИОИ им. П.А Герцена - Филиал ФГБУ «ФМИЦ им. П.А Герцена» Минздрава России; 2015. [Kaprin A.D., Starinskiy V.V., Petrova G.V., eds. Malignancies in Russie in 2013 (morbidity and mortality). Moscow: MNIOI them. PA Herzen - Branch FGBI „FMITS them. PA Herzen „Russian Ministry of Health; 2015. (in Russian)]
  2. Аксель E.M. Статистика злокачественных новообразований женской половой сферы. Онкогинекология. 2012; 1:18-24. [AkselE.M. Statistics of malignant tumors of female genitalia. Onkoginekologiya. 2012; 1: 18-24. (in Russian)]
  3. Солопова A.E., Чащин A.A., Солопова А.Г., Макацария А.Д. Неоадьювантная терапия рака яичников. Современные возможности и критерии отбора. Акушерство, гинекология и репродукция. 2016; 10(2): 44-54. [Solopova А.Е., Chaschin А.А, Solopova A.G., Makatsariya AD. Neoadjuvant therapy of ovarian cancer. Modern features and selection criteria. Akusherstvo, ginekologiya і reproduktsiya. 2016; 10(2): 44-54. (in Russian)]
  4. Gömez-Hidalgo N.R., Martinez-Cannon B.A., Nick A.M., Lu КН., Sood A.K., Coleman R.L., Ramirez RT. Predictors of optimal cytoreduction in patients with newly diagnosed advanced-stage epithelial ovarian cancer: time to incorporate laparoscopic assessment into the standard of care. Gynecol. Oncol. 2015; 137(3): 553-8. doi: 10.1016/j.ygyno.2015.03.049.
  5. Fagö-Olsen C.L., Ottesen B., Kehlet H., Antonsen S.L., Christensen I.J., Markauskas A. et al. Does neoadjuvant chemotherapy impair long-term survival for ovarian cancer patients? A nationwide Danish study. Gynecol. Oncol. 2014; 132(2): 292-8.
  6. Morgan R.J., Armstrong D.K, Alvarez R.D., Bakkum-Gamez J.N. et al. NCCN Clinical Practice Guidelines in Oncology. Ovarian cancer, including fallopian tube cancer and primary peritoneal cancer. Version 2. 2015. Available at: http://www. tri-kobe.org/nccn/guideline/gynecological/english/ovarian.pdf
  7. Sala E., DeSouza N., Lee S.I., Atri M., Hricak H.; Gynaecological Cancer InterGroup. Ovarian cancer: the role of functional imaging as an end point in clinical trials. Int. J. Gynecol. Cancer. 2010; 20(6): 971-8. doi: 10.1111/ IGC.0b013e3181e0a353.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2017 Bionika Media

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies