Magnetic resonance imaging captures the biology of ductal carcinoma in situ.

Journal Article (Journal Article)

PURPOSE: Magnetic resonance imaging (MRI) is an important tool for characterizing invasive breast cancer but has proven to be more challenging in the setting of ductal carcinoma in situ (DCIS). We investigated whether MRI features of DCIS reflect differences in biology and pathology. PATIENTS AND METHODS: Forty five of 100 patients with biopsy-proven DCIS who underwent MRI and had sufficient tissue to be characterized by pathologic (nuclear grade, presence of comedo necrosis, size, and density of disease) and immunohistochemical (IHC) findings (proliferation, Ki67; angiogenesis, CD34; and inflammation, CD68). Pathology and MRI features (enhancement patterns, distribution, size, and density) were analyzed using pairwise and canonical correlations. RESULTS: Histopathologic and IHC variables correlated with MRI features (r = 0.73). The correlation was largely due to size, density (by either MRI or pathology), and inflammation (P < .05). Most small focal masses were estrogen receptor-positive. MRI enhancement patterns that were clumped were more likely than heterogeneous patterns to be high-grade lesions. Homogenous lesions were large, high grade, and rich in macrophages. Presence of comedo necrosis and size could be distinguished on MRI (P < .05). MRI was most likely to over-represent the size of less dense, diffuse DCIS lesions. CONCLUSION: The heterogeneous presentation of DCIS on MRI reflects underlying histopathologic differences.

Full Text

Duke Authors

Cited Authors

  • Esserman, LJ; Kumar, AS; Herrera, AF; Leung, J; Au, A; Chen, Y-Y; Moore, DH; Chen, DF; Hellawell, J; Wolverton, D; Hwang, ES; Hylton, NM

Published Date

  • October 1, 2006

Published In

Volume / Issue

  • 24 / 28

Start / End Page

  • 4603 - 4610

PubMed ID

  • 17008702

Pubmed Central ID

  • PMC4087112

Electronic International Standard Serial Number (EISSN)

  • 1527-7755

Digital Object Identifier (DOI)

  • 10.1200/JCO.2005.04.5518


  • eng

Conference Location

  • United States