Breast masses with peripheral rim enhancement on dynamic contrast-enhancedMR images: Correlation of MR findings with histologic features and expression of growth factors

Citation
R. Matsubayashi et al., Breast masses with peripheral rim enhancement on dynamic contrast-enhancedMR images: Correlation of MR findings with histologic features and expression of growth factors, RADIOLOGY, 217(3), 2000, pp. 841-848
Citations number
33
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
RADIOLOGY
ISSN journal
00338419 → ACNP
Volume
217
Issue
3
Year of publication
2000
Pages
841 - 848
Database
ISI
SICI code
0033-8419(200012)217:3<841:BMWPRE>2.0.ZU;2-3
Abstract
PURPOSE: To investigate the histologic bases of rim enhancement of breast m asses demonstrated on dynamic contrast material-enhanced magnetic resonance (MR) Images. MATERIALS AND METHODS: Dynamic MR images of breast lesions (invasive carcin oma, n = 29; other, n = 6) in 35 women were reviewed. In each patient, subt raction images of the dynamic contrast-enhanced study were obtained, and ea rly and delayed rim enhancement and delayed internal enhancement were evalu ated. The MR findings were correlated with the ratio of microvessel density of the peripheral to the central portion of the lesion, fibrosis, and othe r histologic features, including expression of vascular endothelial growth factor (VECF) and transforming growth factor beta1. RESULTS: Early rim enhancement was observed in 29% and delayed rim enhancem ent was noted in 60% of all patients. Small cancer nests, a high ratio of p eripheral-to-central microvessel density, peripheral VEGF expression, and a low ratio of peripheral-to-central fibrosis were correlated with early rim enhancement. Delayed rim enhancement was correlated with a high degree of fibrosis and inflammatory changes. Delayed internal enhancement was correla ted with a high degree of fibrosis. CONCLUSION: Rim enhancement of breast lesions at MR imaging is due to a com bination of angiogenesis, distribution and degree of fibrosis, expression p attern of VEGF, and various histologic features.