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首页> 外文期刊>Histopathology: Official Journal of the British Division of the International Academy of Pathology >Flat epithelial atypia (DIN 1a, atypical columnar change): an underdiagnosed entity very frequently coexisting with lobular neoplasia.
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Flat epithelial atypia (DIN 1a, atypical columnar change): an underdiagnosed entity very frequently coexisting with lobular neoplasia.

机译:扁平上皮非典型性病变(DIN 1a,非典型柱状改变):一种诊断不足的实体,常与小叶性肿瘤共存。

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摘要

AIMS: Flat epithelial atypia of the breast [FEA; synonyms: ductal intraepithelial neoplasia (DIN) 1a, atypical columnar change] is increasingly recognized by pathologists and shows distinct genetic alterations. The aim of this study was to determine its biological significance as an incidental finding in breast biopsy specimens. METHODS AND RESULTS: On the assumption that both FEA and lobular neoplasia (LN) derive from progenitor cells in the terminal ductal-lobular unit, we investigated the association between FEA and LN semiquantitatively in 111 excisional breast biopsy specimens which contained LN, but did not contain ductal carcinoma in situ (DCIS) or invasive carcinoma. Ninety-six cases (86.5%) revealed coexistence of LN and FEA (P < 0001). The distribution of LN was focal in 41 cases (37%), multifocal in 50 (45%) and extensive in 20 (18%) cases. FEA was identified as focal, multifocal and extensive in 29 (26%), 42 (38%) and 25 (23%) cases, respectively. Distribution patterns of LN and FEA showed no statistically significant correlation. CONCLUSIONS: Due to the striking association between LN and FEA in our material, one may speculate that these two lesions are biologically related and that FEA is an early but non-obligate precursor lesion similar to LN. Based on this assumption, regular clinical and mammographic follow-up of patients with FEA would be prudent.
机译:目的:乳房扁平上皮异型[FEA;同义词:导管上皮内瘤变(DIN)1a,非典型柱状改变]越来越被病理学家所认识,并显示出明显的遗传改变。这项研究的目的是确定其作为乳腺癌活检标本的偶然发现的生物学意义。方法和结果:假设FEA和小叶瘤样增生(LN)均来自末末导管小叶单元的祖细胞,我们半定量研究了111例包含LN但无LN的切除性乳腺活检标本中FEA和LN的关系。包含原位导管癌(DCIS)或浸润性癌。 96例(86.5%)显示LN和FEA共存(P <0001)。 LN的分布集中于41例(37%),多灶50例(45%),广泛分布20例(18%)。 FEA被确定为局灶性,多灶性和广泛性,分别有29例(26%),42例(38%)和25例(23%)。 LN和FEA的分布模式无统计学意义。结论:由于在我们的材料中LN和FEA之间存在惊人的联系,因此我们可以推测这两个病变与生物学相关,FEA是类似于LN的早期但非专性的前体病变。基于此假设,对FEA患者进行定期的临床和乳房X线检查是谨慎的。

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