Clinical and multiparametric MRI signatures of granulomatous prostatitis

被引:28
作者
Rais-Bahrami, Soroush [1 ,2 ]
Nix, Jeffrey W. [1 ]
Turkbey, Baris [3 ]
Pietryga, Jason A. [2 ]
Sanyal, Rupan [2 ]
Thomas, John V. [2 ]
Gordetsky, Jennifer B. [1 ,4 ]
机构
[1] Univ Alabama Birmingham, Dept Urol, Fac Off Tower 1107,510 20th St South, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Radiol, Birmingham, AL 35294 USA
[3] NCI, Mol Imaging Program, NIH, Bethesda, MD 20892 USA
[4] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
关键词
Granuloma; Tuberculosis; Prostate adenocarcinoma; Magnetic resonance imaging; Apparent diffusion coefficient; ULTRASOUND FUSION BIOPSY; TRANSRECTAL ULTRASOUND; ACTIVE SURVEILLANCE; DATA SYSTEM; CANCER; CARCINOMA; DIFFERENTIATION; DISTINCTION; PREDICTION; ACCURACY;
D O I
10.1007/s00261-017-1080-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: The purpose of the study is to differentiate granulomatous prostatitis (GP) from high-grade prostate cancer (PCa) based on clinical findings and imaging characteristics on multiparametric MRI (MP-MRI). Methods: Pathology from patients undergoing MRI/US fusion-guided prostate biopsies between 2014 and 2015 was reviewed. Five patients with biopsy proven GP were identified as well as 15 patients with biopsy-proven Gleason score >= 4 + 3 = 7 PCa. Patients were matched for age, serum PSA level, and prebiopsy-assigned MP-MRI cancer suspicion scores. MP-MRI studies were reviewed to identify findings that would differentiate GP from PCa in patients who had equally high suspicion scores based upon imaging characteristics. Results: All five patients with GP on MR/US fusion-targeted biopsies were assigned a PIRADS 4 or 5 suspicion score. There were equally high suspicion scores on MP-MRI for both groups (p = 0.57). Re-evaluation of the MRI characteristics of the 5 GP patients and 15 matched controls who had pathologically proven Gleason score >= 4 + 3 = 7 PCa on targeted biopsy demonstrated statistically lower mean ADC values within the index targeted lesion for PCa vs. GP (p = 0.002) Qualitatively, no patients with GP on biopsy had imaging evidence of higher-staged disease, while 33% of patients in the high-risk PCa cohort demonstrated at least one high-stage feature (p = 0.003). Conclusion: Patients with GP routinely have MRIs with moderate to high levels of suspicion for harboring PCa. Re-evaluation of these patients' imaging demonstrated characteristics including significantly higher ADC values and absence of high-stage features, which may help differentiate areas of GP from PCa in the future.
引用
收藏
页码:1956 / 1962
页数:7
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