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Incomplete inside-out growth pattern in invasive breast carcinoma: association with lymph vessel invasion and recurrence-free survival.

机译:浸润性乳腺癌内向外生长模式不完全:与淋巴管侵犯和无复发生存相关。

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摘要

Invasive micropapillary carcinoma (IMPC) is a rare subtype of epithelial tumor of the breast listed in the 2003 World Health Organization histologic classification of tumors of the breast. It is characterized by inside-out micropapillary morphology, frequent lymph vessel invasion (LVI), and lymph node metastasis; however, its etiology remains unknown. This study investigated the incomplete inside-out growth pattern (IGP) in invasive ductal carcinoma, not otherwise specified (NOS), and examined the association between incomplete IGP and clinicopathologic features, including the presence of intratumoral lymph vessels (ILV), LVI, nodal metastasis, and prognosis. Tumor tissues from 166 invasive duct carcinomas NOS and 10 IMPCs were immunostained using an anti-epithelial membrane antigen antibody to detect IGP and with D2-40 antibody to determine the presence of ILV and LVI. Incomplete IGP was detected focally in 88 (53%) of 166 invasive duct carcinomas NOS. Transition areas between IMPC and invasive duct carcinoma NOS also showed prominent incomplete IGP in 9 (90%) of 10 IMPCs. Incomplete IGP in invasive duct carcinomas NOS was associated with larger tumor size, higher frequencies of ILV, LVI, nodal metastasis, and poorer recurrence-free survival by univariate analysis. Incomplete IGP, ILV, and tumor size independently affected LVI by multivariate analysis. These findings indicate that incomplete IGP of tumor cell clusters is not uncommon and is a useful tool for predicting LVI in invasive duct carcinoma NOS of the breast.
机译:浸润性微乳头状癌(IMPC)是2003年世界卫生组织对乳腺肿瘤的组织学分类中列出的一种罕见的乳腺上皮肿瘤亚型。它的特征是由内而外的微乳头形态,频繁的淋巴管浸润(LVI)和淋巴结转移。然而,其病因仍然未知。这项研究调查了浸润性导管癌(无其他说明)中不完整的由内而外的生长模式(IGP),并检查了不完整的IGP与临床病理特征之间的关联,包括肿瘤内淋巴管(ILV),LVI,淋巴结的存在转移和预后。使用抗上皮膜抗原抗体检测IGP并使用D2-40抗体免疫I166和LVI,对来自166例浸润性导管癌NOS和10 IMPC的肿瘤组织进行了免疫染色。在166例浸润性导管癌NOS中有88个(53%)局灶性检测到IGP不完全。 IMPC和浸润性导管癌NOS之间的过渡区域在10个IMPC中有9个(90%)也显示出明显的不完全IGP。单因素分析显示,浸润性导管癌中不完全的IGP与更大的肿瘤大小,更高的ILV,LVI频率,淋巴结转移和较差的无复发生存率有关。通过多变量分析,不完整的IGP,ILV和肿瘤大小独立影响LVI。这些发现表明肿瘤细胞簇的不完全IGP并不少见,并且是预测乳腺浸润性导管癌NOS中LVI的有用工具。

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