Diagnostic performance of digital breast tomosynthesis with a wide scan angle compared to full-field digital mammography for the detection and characterization of microcalcifications

Diagnostic performance of digital breast tomosynthesis with a wide scan angle compared to full-field digital mammography for the detection and characterization of microcalcifications
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DOI:
10.1016/j.ejrad.2016.10.004
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发表时间:
2016-12-01
影响因子:
3.3
通讯作者:
Baltzer, Pascal A. T.
Baltzer, Pascal A. T.
中科院分区:
医学3区
文献类型:
--
作者:
Clauser, Paola;Nagl, Georg;Baltzer, Pascal A. T.

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Objectives: To assess the diagnostic performance of digital breast tomosynthesis (DBT), with a wide scan angle, compared to full-field digital mammography (FFDM), for the detection and characterization of microcalcifications.Methods: IRB approval was obtained for this retrospective study. We selected 150 FFDM and DBT (50 benign and 50 malignant histologically verified microcalcifications, 50 cases classified as BI-RADS 1). Four radiologists evaluated, in separate sessions and blinded to patients' history and histology, the presence of microcalcifications. Cases with microcalcifications were assessed for visibility, characteristics, and grade of suspicion using BI-RADS categories. Detection rate and diagnostic performance were calculated. Visibility, lesions' characteristics and reading time were analysed.Results: Detection rate and visibility were good for both FFDM and DBT, without intra-reader differences (P = 0.510). Inter-reader differences were detected (P < 0.018). Only two lesions were not detected by any reader on either FFDM or DBT. Diagnostic performance with DBT was as good as that of FFDM, but a significant inter-reader difference was found (P = 0.041). High inter-reader variability in the use of the descriptors was found. Reading time for DBT was almost twice that for FFDM (44 and 25 s, respectively).Conclusion: Wide scan-angle DBT enabled the detection and characterization of microcalcifications with no significant differences from FFDM. Inter-reader variability was seen. (C) 2016 Elsevier Ireland Ltd. All rights reserved.