Chae Eun Young, Cha Joo Hee, Shin Hee Jung, Choi Woo Jung, Kim Hak Hee
1 All authors: Department of Radiology, Research Institute of Radiology, Asan Medical Center, University of Ulsan, College of Medicine, 388-1 Pungnap-2-dong, Songpa-gu, Seoul 138-736, Korea.
AJR Am J Roentgenol. 2016 Mar;206(3):666-72. doi: 10.2214/AJR.15.14785.
The purpose of this study is to determine the frequency and the malignancy rate of BI-RADS category 3 lesions detected on screening breast ultrasound and to reassess whether they satisfied the requirements of the American College of Radiology Imaging Network (ACRIN) 6666 protocol.
Of 28,796 asymptomatic women who underwent screening mammography during 2 years, 12,187 underwent additional ultrasound as part of the screening. Patients for whom BI-RADS category 3 lesions were seen on the ultrasound were selected. We reviewed the initial ultrasound showing BI-RADS category 3 lesions and mammograms. We also investigated the clinical outcome of these lesions using the reference standard of a combination of pathologic analysis and follow-up for at least 24 months.
The frequency of BI-RADS category 3 lesions detected on screening ultrasound was 14.6% (1783/12,187). Of the 1164 patients with a follow-up duration of at least 24 months or whose lesions were biopsied, eight were eventually proven to have malignancy (0.7%). The malignancy rate was 2.2% (4/184) for patients with abnormal mammograms and 0.4% (4/980) for those with normal mammograms. When the ACRIN 6666 protocols were strictly applied, 225 (19.3%) lesions were retrospectively recategorized as BI-RADS category 4 (n = 12) or category 2 (n = 213). All detected malignancies were early breast cancers with no lymph node metastasis.
Although the frequency of ultrasound BI-RADS category 3 lesions is considerably high (14.6%), the malignancy rate is very low (0.7%), especially in patients with a normal mammogram. Therefore, with BI-RADS category 3 assessment, careful evaluation is required to avoid unnecessary short-interval follow-up or biopsy.
本研究旨在确定筛查乳腺超声检查中BI-RADS 3类病变的发生率及恶性率,并重新评估其是否符合美国放射学会影像网络(ACRIN)6666方案的要求。
在两年内接受筛查乳腺X线摄影的28796名无症状女性中,12187名接受了额外的超声检查作为筛查的一部分。选择超声检查显示为BI-RADS 3类病变的患者。我们回顾了最初显示BI-RADS 3类病变的超声检查和乳腺X线摄影。我们还使用病理分析和至少24个月随访相结合的参考标准,调查了这些病变的临床结局。
筛查超声检查中BI-RADS 3类病变的发生率为14.6%(1783/12187)。在1164名随访时间至少为24个月或病变接受活检的患者中,最终有8例被证实患有恶性肿瘤(0.7%)。乳腺X线摄影异常的患者恶性率为2.2%(4/184),乳腺X线摄影正常的患者恶性率为0.4%(4/980)。当严格应用ACRIN 6666方案时,225例(19.3%)病变被回顾性重新分类为BI-RADS 4类(n = 12)或2类(n = 213)。所有检测到的恶性肿瘤均为无淋巴结转移的早期乳腺癌。
尽管超声BI-RADS 3类病变的发生率相当高(14.6%),但其恶性率非常低(0.7%),尤其是在乳腺X线摄影正常的患者中。因此,对于BI-RADS 3类评估,需要仔细评估以避免不必要的短期随访或活检。