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"High-grade" central acellular carcinoma and matrix-producing carcinoma of the breast: correlation between ultrasonographic findings and pathological features.

Authors :
Yamaguchi R
Tanaka M
Mizushima Y
Hirai Y
Yamaguchi M
Terasaki H
Yokoyama T
Tsuchiya S
Nakashima O
Yano H
Source :
Medical molecular morphology [Med Mol Morphol] 2011 Sep; Vol. 44 (3), pp. 151-7. Date of Electronic Publication: 2011 Sep 16.
Publication Year :
2011

Abstract

High-grade carcinoma with a large central acellular zone (central acellular carcinoma, CAC) and matrixproducing carcinoma (MPC) are aggressive tumors that both have a central myxomatous acellular zone. Their characteristic morphology may be useful in diagnostic imaging. Ultrasonographic findings based on the Breast Imaging Recording and Data System (BI-RADS) and detailed histological features were evaluated in 11 cases of CAC and 2 cases of MPC to characterize their features. Safranin-O staining was undertaken for the evaluation of central acellular zones in these tumors. Overall, ultrasonography demonstrated heterogeneous hyperechoic lesions in the center of the hypoechoic mass. Posterior echo enhancement was observed in all but 1 case. One case was classified as malignant and the others as "borderline." Histologically, cancer tissue was located in the periphery of the tumor with a ring-like structure and fewer cellular central areas comprising hyaline cartilage myxoid material such as those stained by safranin-O. The present study showed that the pathological findings of CACs and MPCs accurately reflect the ultrasonographic findings. Tumors that showed hyperechoic areas in the center of the hypoechoic mass, with posterior echo enhancement indicating acellular zones composed by myxochondroid material, and that were also relatively round on ultrasonography may be benign, but evaluation is required to exclude CAC and MPC.

Details

Language :
English
ISSN :
1860-1499
Volume :
44
Issue :
3
Database :
MEDLINE
Journal :
Medical molecular morphology
Publication Type :
Academic Journal
Accession number :
21922387
Full Text :
https://doi.org/10.1007/s00795-010-0522-3