Britton P D, Flower C D, Freeman A H, Sinnatamby R, Warren R, Goddard M J, Wight D G, Bobrow L
Department of Radiology, Addenbrooke's Hospital and Cambridge University, UK.
Clin Radiol. 1997 Oct;52(10):764-7. doi: 10.1016/s0009-9260(97)80156-0.
We recently changed from using fine needle aspiration cytology to using core biopsy exclusively in the assessment of screen detected abnormalities. Two hundred and two biopsies (1% of women screened) were performed. Surgical histological confirmation was obtained in 111 patients (101 malignant and 10 benign). The remaining patients were either returned to standard 3-yearly screening or early repeat screening after 1 year. Analysis of the results was performed in accordance with the standards specified in the National Health Service Breast Screening Programme (NHSBSP) Publication Number 22. Absolute sensitivity was 89.3%, complete sensitivity was 93.2%, specificity (including patients undergoing both surgical excision and follow-up) was 88.7%. The predictive value of a positive (malignant) core biopsy result was 100%. The false negative rate was 3.9%. Twelve (5.9%) biopsies were classified inadequate for diagnosis. Core biopsy is a safe and accurate way of assessing screen detected abnormalities and can be used as a substitute for fine needle aspiration cytology with results that exceed the National Health Service Breast Screening Programme target standards, even in the learning phase.
我们最近在筛查发现的异常评估中,从使用细针穿刺细胞学检查改为仅使用粗针活检。共进行了202例活检(占筛查女性的1%)。111例患者(101例恶性和10例良性)获得了手术组织学确诊。其余患者要么恢复标准的三年一次筛查,要么在1年后进行早期重复筛查。根据英国国家医疗服务体系乳腺筛查计划(NHSBSP)第22号出版物规定的标准对结果进行分析。绝对灵敏度为89.3%,完全灵敏度为93.2%,特异性(包括接受手术切除和随访的患者)为88.7%。粗针活检结果为阳性(恶性)的预测值为100%。假阴性率为3.9%。12例(5.9%)活检被判定为诊断不充分。粗针活检是评估筛查发现异常的一种安全且准确的方法,即使在学习阶段,也可作为细针穿刺细胞学检查的替代方法,其结果超过了英国国家医疗服务体系乳腺筛查计划的目标标准。