不确定恶性潜能的B3乳腺病变的异质性风险概况

P. Orsaria, A. Grasso, Rita Carino, E. Caredda, M. Sammarra, C. Altomare, C. Rabitti, G. Gullotta, G. Perrone, F. Pantano, O. Buonomo, V. Altomare
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引用次数: 15

摘要

背景:大多数乳腺恶性潜能不确定的病变(B3)接受手术治疗。我们的目的是分析大量筛查检测病例中B3病变亚型的结果。方法:筛选2986例核心穿刺活检,对B3病变进行分类。根据临床病理和形态学变量计算恶性肿瘤的阳性预测值(PPVs),以进行全面的风险表征。结果:B3病变包括35%的不典型导管增生(PPV = 20%), 16.7%的扁平上皮异型增生(PPV = 12%), 22.7%的小叶瘤变(PPV = 16.2%), 9%的乳头状病变(PPV = 18.5%), 8.6%的叶状瘤(PPV = 3.8%), 8%的放射状疤痕(PPV = 4.1%)。钙化升级率为15.9%,肿块升级率为13.7%,建筑畸形升级率为16.7%,其中8.3%的恶性病变为导管原位癌,6.7%为浸润性癌(PPV = 15%)。结论:B3型病变具有异质性的恶性风险,需要仔细的影像学和病理学联系才能获得最佳治疗。
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Heterogeneous risk profiles among B3 breast lesions of uncertain malignant potential
Background: Most cases of breast lesions of uncertain malignant potential (B3) undergo surgical intervention. We aimed to analyze the outcome of B3 lesion subtypes in a large series of screen-detected cases. Methods: We screened 2,986 core needle biopsies to classify B3 lesions. Positive predictive values (PPVs) for malignancy were calculated for a comprehensive risk characterization according to clinicopathologic and morphologic variables. Results: B3 lesions comprised 35% atypical ductal hyperplasia (PPV = 20%), 16.7% flat epithelial atypia (PPV = 12%), 22.7% lobular neoplasia (PPV = 16.2%), 9% papillary lesion (PPV = 18.5%), 8.6% phyllodes tumor (PPV = 3.8%), and 8% radial scars (PPV = 4.1%) based on histopathologic diagnosis. Upgrade rates were 15.9% for calcifications, 13.7% for mass lesions, and 16.7% for architectural deformities, with 8.3% of malignant lesions classified as ductal carcinoma in situ and 6.7% as invasive cancers (PPV = 15%). Conclusion: B3 lesions entail a heterogeneous risk of malignancy, and careful radiologic–pathologic correlation is required for optimal treatment.
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