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现行的胎盘部位结节不典型病变标准的应用提示需要更精细的标准。

Application of Current Pathologic Criteria for Atypical Placental Site Nodule Suggests That Refined Criteria Are Needed.

出版信息

Int J Gynecol Pathol. 2023 Sep 1;42(5):482-490. doi: 10.1097/PGP.0000000000000934. Epub 2023 Jan 3.

Abstract

Atypical placental site nodules (APSNs) are histologically intermediate between placental site nodules (PSNs) and epithelioid trophoblastic tumors (ETTs). Little data exists to characterize these lesions and the risk of transformation from PSN to ETT. Recent World Health Organization (WHO) criteria for distinction of APSN are vague and not objectively defined. We identified cases signed out as PSN (n=33) and APSN (n=11) and aimed to characterize, statistically compare, and assess the risk of transformation in PSNs using data including size, location, mitotic rate, Ki-67 proliferation index, trophoblastic cells per high-power field, presence of severe cytologic atypia, beta-human chorionic gonadotropin levels, time since last pregnancy, presence of calcification, necrosis, or apoptosis, and follow-up results. All cases were confirmed to be positive for p63, and a Ki-67/AE1/AE3 dual stain was used to evaluate the Ki-67 proliferation index in the trophoblastic cells. In our cohort, slight changes in the interpretation of WHO criteria for PSN and APSN led to marked differences in the proportion of PSNs flagged as "atypical." There was no statistically significant difference in the persistence of APSN versus non-APSN. None of the PSNs transformed to ETT. Current criteria for distinction between PSN and APSN are largely subjective. More objective, clearly defined, and clinically meaningful criteria are needed to distinguish between PSN and APSN, thus aiding in assessing the rare risk of transformation to ETT.

摘要

不典型胎盘部位结节(APSN)在组织学上介于胎盘部位结节(PSN)和上皮样滋养细胞肿瘤(ETT)之间。关于这些病变以及 PSN 向 ETT 转化的风险,目前的数据很少。最近世界卫生组织(WHO)对 APSN 进行区分的标准比较模糊,也没有明确定义。我们鉴定了病理报告为 PSN(n=33)和 APSN(n=11)的病例,旨在通过大小、位置、有丝分裂率、Ki-67 增殖指数、高倍视野中滋养细胞数量、存在严重细胞学异型性、β-人绒毛膜促性腺激素水平、上次妊娠后时间、有无钙化、坏死或凋亡以及随访结果等数据,对 PSN 进行特征描述、统计学比较和转化风险评估。所有病例均证实 p63 阳性,并使用 Ki-67/AE1/AE3 双重染色来评估滋养细胞中的 Ki-67 增殖指数。在我们的研究中,对 PSN 和 APSN 的 WHO 标准的解释稍有变化,就会导致被标记为“不典型”的 PSN 的比例有显著差异。APSN 与非 APSN 持续存在的比例没有统计学差异。没有 PSN 转化为 ETT。目前区分 PSN 和 APSN 的标准在很大程度上是主观的。需要更客观、明确和有临床意义的标准来区分 PSN 和 APSN,从而有助于评估向 ETT 转化的罕见风险。

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