Spectroscopic Imaging (1H-2D-CSl) of the prostate:: sequence optimization and correlation with histophatological results.

被引:7
作者
Stanka, M
Eltze, E
Semjonow, A
Sievert, KD
Maier, A
Pfleiderer, B
机构
[1] Univ Munster, Inst Klin Radiol, D-48129 Munster, Germany
[2] Univ Munster, Gerhard Domagk Inst Pathol, D-48129 Munster, Germany
[3] Univ Munster, Klin & Poliklin Urol, D-48129 Munster, Germany
来源
ROFO-FORTSCHRITTE AUF DEM GEBIET DER RONTGENSTRAHLEN UND DER BILDGEBENDEN VERFAHREN | 2000年 / 172卷 / 07期
关键词
prostate; MR; neoplasia; magnetic resonance (MR) spectroscopy; H-1 MR spectroscopic imaging; prostate cancer; tumor detection; tumor grading; prostatic intraepithelial neoplasia;
D O I
10.1055/s-2000-4644
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: Methodological optimization of a H-1 MR spectroscopic imaging sequence (H-1-2D-CSI) and evaluation of its potential to diagnose prostate cancer as validated by histopathological maps, Methods: The prostates of 18 patients were evaluated by H-1-MR-CSI (voxel dimension: 1 cm(3)) at 1,5 Tesla, This sequence was additionally combined with a frequency selective fat suppression. Results: it was possible to distinguish prostate carcinoma from prostate hyperplasia spectroscopically by the ratio of citrate/(choline + creatine). Differentiation of high-grade prostatic intraepithelial neoplasia (PIN, high-grade) from prostate carcinoma was not unambiguously possible. Prediction of tumor differentiation was not possible by the ratio of citrate/(choline + creatine) by our maximum spatial resolution of 1 cm(3). Conclusion: H-1-2D-CSI is suitable for tumor detection. Tumor differentiation was not possible with the spatial resolution used.
引用
收藏
页码:623 / 629
页数:7
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