The diverse pathology and kinetics of mass, nonmass, and focus enhancement on MR imaging of the breast
Purpose: To compare the pathology and kinetic characteristics of breast lesions with focus‐, mass‐, and nonmass‐like enhancement. Materials and Methods: A total of 852 MRI detected breast lesions in 697 patients were selected for an IRB approved review. Patients underwent dynamic contrast enhanced M...
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Published in | Journal of magnetic resonance imaging Vol. 33; no. 6; pp. 1382 - 1389 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.06.2011
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Subjects | |
Online Access | Get full text |
ISSN | 1053-1807 1522-2586 1522-2586 |
DOI | 10.1002/jmri.22567 |
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Summary: | Purpose:
To compare the pathology and kinetic characteristics of breast lesions with focus‐, mass‐, and nonmass‐like enhancement.
Materials and Methods:
A total of 852 MRI detected breast lesions in 697 patients were selected for an IRB approved review. Patients underwent dynamic contrast enhanced MRI using one pre‐ and three to six postcontrast T1‐weighted images. The “type” of enhancement was classified as mass, nonmass, or focus, and kinetic curves quantified by the initial enhancement percentage (E1), time to peak enhancement (Tpeak), and signal enhancement ratio (SER). These kinetic parameters were compared between malignant and benign lesions within each morphologic type.
Results:
A total of 552 lesions were classified as mass (396 malignant, 156 benign), 261 as nonmass (212 malignant, 49 benign), and 39 as focus (9 malignant, 30 benign). The most common pathology of malignant/benign lesions by morphology: for mass, invasive ductal carcinoma/fibroadenoma; for nonmass, ductal carcinoma in situ (DCIS)/fibrocystic change(FCC); for focus, DCIS/FCC. Benign mass lesions exhibited significantly lower E1, longer Tpeak, and lower SER compared with malignant mass lesions (P < 0.0001). Benign nonmass lesions exhibited only a lower SER compared with malignant nonmass lesions (P < 0.01).
Conclusion:
By considering the diverse pathology and kinetic characteristics of different lesion morphologies, diagnostic accuracy may be improved. J. Magn. Reson. Imaging 2011;33:1382–1389. © 2011 Wiley‐Liss, Inc. |
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Bibliography: | ark:/67375/WNG-J8TVPWK1-9 ArticleID:JMRI22567 NIH - No. P50 CA125183-01 (SPORE) Segal Foundation Department of Defense - No. Predoctoral Award WX81XWH-06-1-0329 istex:5BCB352444D4C0AFC9A32A74861FBAA1266067EC ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Currently at Mouse Cancer Genetics Program, National Cancer Institute, Frederick Maryland |
ISSN: | 1053-1807 1522-2586 1522-2586 |
DOI: | 10.1002/jmri.22567 |