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基于基底细胞和结构模式对非典型前列腺上皮内病变进行分层。

Stratification of Atypical Intraepithelial Prostatic Lesions Based on Basal Cell and Architectural Patterns.

机构信息

Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles.

出版信息

Am J Clin Pathol. 2020 Feb 8;153(3):407-416. doi: 10.1093/ajcp/aqz183.

Abstract

OBJECTIVES

High-grade prostatic intraepithelial neoplasia (HPIN) and atypical cribriform lesion of the prostate are considered the precursors or associators of invasive prostate cancer (iPCa). Given loss of basal cells being the hallmark of iPCa, we hypothesized that a subset of these atypical intraepithelial lesions (AILs) with sparse basal cells can be classified as prostatic intraepithelial carcinoma (PIC) with frequent iPCa association and that different morphologic patterns of PIC are associated with specific Gleason (G) patterns and scores for iPCa.

METHODS

We stratified 153 foci of AILs from 110 patients based on the integrity of the basal cell layer and architectural patterns and their association with iPCa.

RESULTS

We demonstrated that AILs could be stratified into usual HPIN (intact basal cell layer and simple patterns) with low-risk of iPCa association and PIC (sparse basal cell layer) with high risk of iPCa association. Furthermore, PIC could be divided into low-grade (simple patterns and associated with G3 and G3/4 iPCa) and high-grade PIC (complex patterns and associated with G4 and G3/4/5 iPCa).

CONCLUSIONS

Such stratification is of great clinical significance and instrumental to clinical patient management. It not only increases the predictability of AILs for iPCa but also accommodates a clinical scenario for lesions with features of intraductal carcinoma when iPCa is not found, particularly in biopsies.

摘要

目的

高级前列腺上皮内瘤变(HPIN)和前列腺非典型筛状病变被认为是浸润性前列腺癌(iPCa)的前体或伴发病变。鉴于基底细胞缺失是 iPCa 的标志,我们假设这些具有稀疏基底细胞的不典型上皮内病变(AILs)中的一部分可以被归类为具有频繁 iPCa 相关性的前列腺上皮内癌(PIC),并且不同形态学模式的 PIC 与特定的 Gleason(G)模式和 iPCa 评分相关。

方法

我们根据基底细胞层的完整性和结构模式以及它们与 iPCa 的关联,对 110 名患者的 153 个 AIL 病灶进行分层。

结果

我们表明,AILs 可以分为具有低 iPCa 相关性的通常的 HPIN(完整的基底细胞层和简单模式)和具有高 iPCa 相关性的 PIC(稀疏基底细胞层)。此外,PIC 可分为低级别(简单模式,与 G3 和 G3/4 iPCa 相关)和高级别 PIC(复杂模式,与 G4 和 G3/4/5 iPCa 相关)。

结论

这种分层具有重要的临床意义,有助于临床患者管理。它不仅增加了 AILs 对 iPCa 的预测性,而且还为在未发现 iPCa 时具有导管内癌特征的病变提供了一种临床情况,特别是在活检中。

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