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LOWER GENITOURINARY TRACT IMAGING |
1 From the Department of Radiology, Memorial Sloan-Kettering Cancer Center, 1275 York Ave, C278, New York, NY 10021 (F.G.C., H.H.); and Department of Diagnostic Radiology, University of Arizona, Tucson (R.R.H.). Received March 30, 2004; revision requested April 19; revision received May 5 and accepted May 11. All authors have no financial relationships to disclose. Supported by National Institutes of Health grant R01 CA76423. Address correspondence to F.G.C. (e-mail: clausf@mskcc.org).
Magnetic resonance (MR) imaging and hydrogen 1 MR spectroscopy of the prostate gland are performed during the same examination with a conventional clinical MR unit. Prostate zonal anatomy and prostate cancer are best depicted on multiplanar T2-weighted MR images. MR imaging and 1H MR spectroscopy are not used as an initial diagnostic tool. Their use in tumor detection is reserved for patients with elevated prostate-specific antigen levels in whom previous biopsy results were negative. The use of MR imaging and 1H MR spectroscopy for the evaluation of tumor location, local extent (extracapsular extension and/or seminal vesicle invasion), volume, and aggressiveness is generating strong clinical interest. In staging and treatment planning, MR imaging has been shown to have an incremental value additive to the value of clinical nomograms. Furthermore, anatomic and metabolic mapping of the prostate gland with 1H MR spectroscopy offers the possibility of optimizing treatment planning (watchful waiting, surgery, or radiation therapy [intensity-modulated radiation therapy or brachytherapy]), thus further expanding the role of MR imaging in the achievement of patient-specific, individualized treatment.
© RSNA, 2004
Index Terms: Neoplasms, staging, 844.1214, 844.12145 Prostate neoplasms, MR, 844.1214, 844.12145
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