David Odile, Cabay Robert J, Pasha Seema, Dietrich Ruth, Leach Lu, Guo Meihua, Mehrotra Swati
Department of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
Cancer. 2009 Jun 25;117(3):157-66. doi: 10.1002/cncy.20020.
Discordant results of cervical biopsy histology after a cytologic diagnosis of high-grade squamous intraepithelial lesion (HSIL) are often attributed to sampling variation. The purpose of the current study was to determine whether deeper levels and ancillary staining (p16(Ink4a) and ProExC) reduce the discordant rate.
A total of 246 cases of HSIL were retrieved from the computerized database from 2005 and 2006. Of these cases, 151 were followed by cervical biopsy. There was cytologic-histologic correlation in 87 cases, as defined by the presence of high-grade (2 or 3) cervical intraepithelial neoplasia (HGCIN). For each discordant biopsy (n = 64), 2 deeper levels for hematoxylin and eosin (H&E) were taken at 30-micro and 90-micro depths, and 4 sections for p16(Ink4a) and ProExC staining were taken at a 60-micro depth. All cytologic and histologic material from these 64 cases was reviewed by 3 cytopathologists. In 2 cases, the original HSIL diagnoses were downgraded and the cases censored from the study.
Fifty-seven of the 62 discordant cases had sufficient tissue for deeper levels and ancillary staining. Two of 57 cases were reclassified to HGCIN. In both of these cases, reclassification was suggested by results of immunostains; however, the H&E sections were necessary for definitive interpretation of the immunostain results.
In the current study, deeper levels and ancillary staining with p16(Ink4a) and ProExC did not significantly reduce the discordance rate. Although there are many known causes of sampling variation, including factors related to colposcopic technique, regression of infection, and insufficient histologic sectioning, sampling variation remains a valid justification of noncorrelation in women with HSIL followed up by cervical biopsy alone.
在细胞学诊断为高级别鳞状上皮内病变(HSIL)后,宫颈活检组织学结果不一致通常归因于取样差异。本研究的目的是确定更深层次的切片及辅助染色(p16(Ink4a)和ProExC)是否能降低不一致率。
从2005年和2006年的计算机数据库中检索出246例HSIL病例。其中151例随后进行了宫颈活检。87例存在细胞学与组织学相关性,定义为存在高级别(2级或3级)宫颈上皮内瘤变(HGCIN)。对于每例不一致的活检病例(n = 64),在30微米和90微米深度处取2个更深层次的苏木精和伊红(H&E)切片,在60微米深度处取4个用于p16(Ink4a)和ProExC染色的切片。这64例病例的所有细胞学和组织学材料由3位细胞病理学家进行复查。2例病例中,最初的HSIL诊断被降级,这2例病例从研究中剔除。
62例不一致病例中的57例有足够的组织用于更深层次的切片及辅助染色。57例中有2例被重新分类为HGCIN。在这2例病例中,免疫染色结果提示了重新分类;然而,H&E切片对于免疫染色结果的最终解读是必要的。
在本研究中,更深层次的切片及p16(Ink4a)和ProExC辅助染色并未显著降低不一致率。尽管存在许多已知的取样差异原因,包括与阴道镜检查技术、感染消退以及组织学切片不足相关的因素,但取样差异仍然是仅接受宫颈活检随访的HSIL女性中出现不相关性的一个合理原因。