Burns R P, Brown J P, Roe S M, Sprouse L R, Yancey A E, Witherspoon L E
Department of Surgery, University of Tennessee College of Medicine, Chattanooga Unit, Chattanooga, Tennessee 37403, USA.
Ann Surg. 2000 Oct;232(4):542-8. doi: 10.1097/00000658-200010000-00009.
To evaluate the reliability of stereotactic core-needle breast biopsy (SCNB) performed by surgeons to detect histologically benign tissue.
Stereotactic core-needle breast biopsy is widely used to obtain tissue for definitive pathologic diagnosis of mammographically suspicious breast lesions. It has an incidence of malignancy detection similar to that of open biopsy. The potential for sampling error is a concern. Minimal data regarding follow-up and failure rate are available, especially from series performed exclusively by surgeons.
Pertinent medical records of all patients who underwent SCNB between April 1995 and October 1997 were reviewed. Breast lesions were classified by mammographic Breast Imaging-Reporting and Data Systems (BI-RADS) categories before SCNB. Benign biopsy specimens were classified as nonproliferative or proliferative. Malignant lesions and those with atypical histopathology by SCNB were excluded from this analysis. All lesions initially reported as benign were followed up mammographically for at least 2 years for any suspicious change requiring repeat biopsy.
During the 31-month period, SCNB was performed on 694 lesions in 619 patients. Histologic evidence of malignancy was found in 112 lesions (16%). The initial histologic diagnosis for the remaining 582 lesions was benign. Four hundred lesions were available for follow-up; of these, 373 (93%) were mammographically categorized as BI-RADS 3 (probably benign) or 4 (suspicious). Three hundred forty-three lesions were categorized as nonproliferative and 151 as proliferative (94 had combined nonproliferative and proliferative histology). Follow-up ranged from 24 to 48 months (mean 33 months). During the follow-up period, 87 lesions (21.8%) underwent either image-guided or open biopsy. At the time of follow-up rebiopsy, ductal carcinoma in situ was found in four lesions and infiltrating ductal carcinoma was found in one, for an overall false-negative rate of 4.3% (5/117) and a negative predictive value of 98.8% (395/400). For the five false-negative cases, the interval from initial SCNB to definitive diagnosis ranged from 7 to 36 months. No correlation was found between the type of initial histopathology and development of malignancy.
These results support SCNB as an alternative to open biopsy and show the reliability of SCNB when benign pathology is obtained. However, given the possibility of sampling error and the nature of breast disease, close mammographic and clinical follow-up is necessary. The false-negative rate and negative predictive value in this series compare favorably with those in other reports, supporting the fact that surgeons can confidently use SCNB in the evaluation and treatment of breast disease.
评估外科医生进行的立体定向芯针乳腺活检(SCNB)检测组织学良性组织的可靠性。
立体定向芯针乳腺活检广泛用于获取组织,以对乳腺钼靶检查可疑的乳腺病变进行明确的病理诊断。其恶性肿瘤检出率与开放活检相似。采样误差的可能性令人担忧。关于随访和失败率的可用数据极少,尤其是来自仅由外科医生进行的系列研究。
回顾了1995年4月至1997年10月期间所有接受SCNB的患者的相关医疗记录。在SCNB前,根据乳腺钼靶影像报告和数据系统(BI-RADS)类别对乳腺病变进行分类。良性活检标本分为非增殖性或增殖性。本分析排除了恶性病变和SCNB显示非典型组织病理学的病变。所有最初报告为良性的病变均进行乳腺钼靶随访至少2年,以观察是否有任何需要重复活检的可疑变化。
在31个月期间,对619例患者的694个病变进行了SCNB。112个病变(16%)发现有恶性组织学证据。其余582个病变的初始组织学诊断为良性。400个病变可供随访;其中,373个(93%)在乳腺钼靶检查中分类为BI-RADS 3(可能良性)或4(可疑)。343个病变分类为非增殖性,151个为增殖性(94个具有非增殖性和增殖性混合组织学)。随访时间为24至48个月(平均33个月)。在随访期间,87个病变(21.8%)接受了影像引导或开放活检。在随访再次活检时,4个病变发现原位导管癌,1个发现浸润性导管癌,总体假阴性率为4.3%(5/117),阴性预测值为98.8%(395/400)。对于5例假阴性病例,从初始SCNB到明确诊断的间隔时间为7至36个月。未发现初始组织病理学类型与恶性肿瘤发生之间的相关性。
这些结果支持SCNB作为开放活检的替代方法,并表明获得良性病理时SCNB的可靠性。然而,鉴于存在采样误差的可能性和乳腺疾病性质,密切的乳腺钼靶和临床随访是必要的。本系列中的假阴性率和阴性预测值与其他报告相比具有优势,支持外科医生可以自信地在乳腺疾病评估和治疗中使用SCNB这一事实。