乳房核心穿刺活检中扁平上皮异型性与影像学病理一致

Anne Grabenstetter, Sandra B Brennan, E. D. Salagean, M. Morrow, E. Brogi
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引用次数: 14

摘要

扁平上皮异型性(FEA)是由低级别异型性导管上皮增生引起的末端导管小叶单位的改变。核心穿刺活检(CNB)中FEA的诊断是否需要切除(EXC)尚无共识。我们回顾性地确定了2012年1月至2018年7月期间通过FEA获得的所有内部cnb。我们回顾了所有的CNB切片,并评估了放射学和病理学的一致性。升级定义为EXC中的浸润性癌(IC)和/或导管原位癌。我们回顾了所有升级病例的EXC切片。在研究期间的15700例连续cnb中,106例患者的106例cnb单独产生FEA或伴有典型小叶瘤变(LN)。我们排除了52例cnb(40例既往/并发癌患者和12例无EXC患者)。经复查,我们对14例进行了重新分类,其中2例为核非典型增生,10例为局灶性非典型导管增生,2例为良性。最终的FEA研究队列包括来自40名女性的40个cnb。36例(90%)为CNB靶性乳房x线钙化,3例(8%)为磁共振非肿块增强,1例(2%)为超声肿块。所有CNBs均被认为是放射-病理一致的。34个cnb中仅存在FEA, 6个cnb中存在LN。EXC产生2个低级别IC,每个跨越< 2mm,在组织切片中发现,没有活检部位改变。其余38例无升级。经典LN不影响升级。有限元升级率为5%;两种都是微小的、低级别的“偶发”IC。我们的结论是,对于没有既往/并发癌且放射-病理一致性CNB诊断为FEA的患者,可以考虑非手术治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Flat Epithelial Atypia in Breast Core Needle Biopsies With Radiologic-Pathologic Concordance
Flat epithelial atypia (FEA) is an alteration of terminal duct lobular units by a proliferation of ductal epithelium with low-grade atypia. No consensus exists on whether the diagnosis of FEA in core needle biopsy (CNB) requires excision (EXC). We retrospectively identified all in-house CNBs obtained between January 2012 and July 2018 with FEA. We reviewed all CNB slides and assessed radiologic-pathologic concordance. An upgrade was defined as invasive carcinoma (IC) and/or ductal carcinoma in situ in the EXC. The EXC slides of all upgraded cases were rereviewed. Out of ∼15,700 consecutive CNBs in the study period, 106 CNBs from 106 patients yielded FEA alone or with classic lobular neoplasia (LN). We excluded 52 CNBs (40 patients with prior/concurrent carcinoma and 12 without EXC). After rereview, we reclassified 14 cases (2 marked nuclear atypia, 10 focal atypical ductal hyperplasia, 2 benign). The final FEA study cohort consisted of 40 CNBs from 40 women. The CNB targeted mammographic calcifications in 36 (90%) cases, magnetic resonance imaging nonmass enhancement in 3 (8%), and 1 (2%) sonographic mass. All CNBs were deemed radiologic-pathologic concordant. FEA was present alone in 34 CNBs and with LN in 6. EXC yielded 2 low-grade IC, each spanning <2 mm, identified in tissue sections without biopsy site changes. The remaining 38 cases had no upgrade. Classic LN did not affect the upgrade. The upgrade rate of FEA was 5%; both minute, low-grade “incidental” IC. We conclude that nonsurgical management may be considered in patients without prior/concurrent carcinoma and radiologic-pathologic concordant CNB diagnosis of FEA.
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