Sep, 2007
Assessment of the vascularity of uterine leiomyomas using double-echo dynamic perfusion-weighted MRI with the first-pass pharmacokinetic model - Correlation with histopathology
INVESTIGATIVE RADIOLOGY
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- Volume
- 42
- Number
- 9
- First page
- 629
- Last page
- 635
- Language
- English
- Publishing type
- Research paper (scientific journal)
- DOI
- 10.1097/RLI.0b013e318059ae69
- Publisher
- LIPPINCOTT WILLIAMS & WILKINS
Objectives: To retrospectively evaluate the feasibility of perfusion-weighted MRI (PWI) in uterine leiomyomas.
Materials and Methods: Eighteen uterine leiomyomas in 15 patients were evaluated. PWI was performed using a double-echo T2*-weighted spoiled gradient-recalled acquisition sequence, and the first-pass pharmacokinetic model was applied to calculate relative blood volume (rBV). Histopathologic analysis was performed to measure vascular area (VA).
Results: PWI was successful in 13 of 15 patients. On quantitative analysis, mean (+/- SD) rBV calculated from PWI was 0.17 +/- 0.13 (range, 0.06-0.55), whereas mean VA was 3.3% +/- 1.6% (range, 1.7-8.5%). A significant correlation was identified between rBV and VA (r = 0.87, P < 0.001).
Conclusions: The rBV determined at PWI correlates with histologic vascular area in uterine leiomyomas.
Materials and Methods: Eighteen uterine leiomyomas in 15 patients were evaluated. PWI was performed using a double-echo T2*-weighted spoiled gradient-recalled acquisition sequence, and the first-pass pharmacokinetic model was applied to calculate relative blood volume (rBV). Histopathologic analysis was performed to measure vascular area (VA).
Results: PWI was successful in 13 of 15 patients. On quantitative analysis, mean (+/- SD) rBV calculated from PWI was 0.17 +/- 0.13 (range, 0.06-0.55), whereas mean VA was 3.3% +/- 1.6% (range, 1.7-8.5%). A significant correlation was identified between rBV and VA (r = 0.87, P < 0.001).
Conclusions: The rBV determined at PWI correlates with histologic vascular area in uterine leiomyomas.
- Link information
- ID information
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- DOI : 10.1097/RLI.0b013e318059ae69
- ISSN : 0020-9996
- Pubmed ID : 17700278
- Web of Science ID : WOS:000248931600004