TY - JOUR
T1 - Microcalcification morphological descriptors and parenchyma fractal dimension hierarchically interact in breast cancer
T2 - A diagnostic perspective
AU - Verma, Garima
AU - Luciani, Maria Laura
AU - Palombo, Alessandro
AU - Metaxa, Linda
AU - Panzironi, Giovanna
AU - Pediconi, Federica
AU - Giuliani, Alessandro
AU - Bizzarri, Mariano
AU - Todde, Virginia
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Introduction Herein, we propose a Systems Biology approach aimed at identifying quantitative morphological parameters useful in discriminating benign from malignant breast microcalcifications at digital mammography. Materials and methods The study includes 31 patients in which microcalcifications had been detected during XR mammography and were further confirmed by stereotactic (XR-guided) biopsies. Patients were classified according to the BIRADS (Breast Imaging-Reporting and Data System), along with their parenchyma fractal dimension and biopsy size. A geometrical-topological characterization of microcalcifications was obtained as well. Results The 'size of biopsy’ was the parameter endowed with the highest discriminant power between malignant and benign lesions thus confirming the reliability of surgeon judgment. The quantitative shape evaluation of both lesions and parenchyma allowed for a promising prediction of the BIRADS score. The area of lesions and parenchyma fractal dimension show a complex distribution for malignant breast calcifications that are consistent with their qualitative morphological pattern. Fractal dimension analysis enables the user to obtain reliable results as proved by its efficiency in the prediction of the morphology of breast cancer. Conclusion By reconstructing a phase-space distribution of biophysical parameters, different patterns of aggregation are recognized corresponding to different calcium deposition patterns, while the combination of tissue and microcalcification morphological descriptors provide a statistically significant prediction of tumour grade. Clinical relevance The development of an automated morphology evaluation system can help during clinical evaluation while also sketching mechanistic hypotheses of microcalcification generation.
AB - Introduction Herein, we propose a Systems Biology approach aimed at identifying quantitative morphological parameters useful in discriminating benign from malignant breast microcalcifications at digital mammography. Materials and methods The study includes 31 patients in which microcalcifications had been detected during XR mammography and were further confirmed by stereotactic (XR-guided) biopsies. Patients were classified according to the BIRADS (Breast Imaging-Reporting and Data System), along with their parenchyma fractal dimension and biopsy size. A geometrical-topological characterization of microcalcifications was obtained as well. Results The 'size of biopsy’ was the parameter endowed with the highest discriminant power between malignant and benign lesions thus confirming the reliability of surgeon judgment. The quantitative shape evaluation of both lesions and parenchyma allowed for a promising prediction of the BIRADS score. The area of lesions and parenchyma fractal dimension show a complex distribution for malignant breast calcifications that are consistent with their qualitative morphological pattern. Fractal dimension analysis enables the user to obtain reliable results as proved by its efficiency in the prediction of the morphology of breast cancer. Conclusion By reconstructing a phase-space distribution of biophysical parameters, different patterns of aggregation are recognized corresponding to different calcium deposition patterns, while the combination of tissue and microcalcification morphological descriptors provide a statistically significant prediction of tumour grade. Clinical relevance The development of an automated morphology evaluation system can help during clinical evaluation while also sketching mechanistic hypotheses of microcalcification generation.
KW - Fractal dimension
KW - Mammography
KW - Microcalcification
KW - Quantitative morphology
KW - Radiology
KW - Systems biology
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U2 - 10.1016/j.compbiomed.2017.12.004
DO - 10.1016/j.compbiomed.2017.12.004
M3 - Article
C2 - 29247886
AN - SCOPUS:85038030093
SN - 0010-4825
VL - 93
SP - 1
EP - 6
JO - Computers in Biology and Medicine
JF - Computers in Biology and Medicine
ER -