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ARID1B免疫组织化学是诊断去分化和未分化妇科恶性肿瘤的重要检测方法。

ARID1B Immunohistochemistry Is an Important Test for the Diagnosis of Dedifferentiated and Undifferentiated Gynecologic Malignancies.

作者信息

Tessier-Cloutier Basile

机构信息

Department of Pathology, McGill University, Montreal, QC H3A 2B4, Canada.

Division of Pathology, McGill University Health Centre, Montreal, QC H4A 3J1, Canada.

出版信息

Cancers (Basel). 2023 Aug 24;15(17):4229. doi: 10.3390/cancers15174229.

Abstract

Dedifferentiated and undifferentiated endometrial and ovarian carcinomas (DDC/UDC) are aggressive malignancies defined by morphologic and molecular undifferentiation, and associated with core SWI/SNF deficiency. Their main differential diagnoses include high-grade endometrial and ovarian carcinomas that often show overlapping morphologic and molecular profiles. Loss of cell lineage markers expression by immunohistochemistry (IHC) is commonly used to assist diagnosis, but it has poor specificity, while core SWI/SNF deficiency is much more specific. Approximately half of SWI/SNF-deficient DDC/UDC are associated with loss of ARID1B expression, yet, unlike the other core SWI/SNF proteins (SMARCA4 and SMARCB1), this test is rarely available, even in tertiary centers. Mutational testing for ARID1B is increasingly common among targeted DNA sequencing panels, but it is difficult to interpret in the absence of IHC results. Overall, the importance of including ARID1B IHC as part of the routine panel for undifferentiated gynecologic malignancies should be emphasized, especially as SWI/SNF inactivation is becoming a necessary biomarker for diagnostics, clinical management, and clinical trial enrollment.

摘要

去分化和未分化子宫内膜癌及卵巢癌(DDC/UDC)是侵袭性恶性肿瘤,其定义为形态学和分子水平的未分化,并与核心SWI/SNF缺陷相关。它们的主要鉴别诊断包括高级别子宫内膜癌和卵巢癌,这些肿瘤常表现出形态学和分子特征的重叠。通过免疫组织化学(IHC)检测细胞谱系标志物表达缺失常用于辅助诊断,但其特异性较差,而核心SWI/SNF缺陷的特异性要强得多。大约一半的SWI/SNF缺陷型DDC/UDC与ARID1B表达缺失有关,然而,与其他核心SWI/SNF蛋白(SMARCA4和SMARCB1)不同,即使在三级医疗中心,这项检测也很少能做。ARID1B的突变检测在靶向DNA测序检测中越来越普遍,但在没有IHC结果的情况下很难解读。总体而言,应强调将ARID1B IHC纳入未分化妇科恶性肿瘤常规检测项目的重要性,尤其是因为SWI/SNF失活正成为诊断、临床管理和临床试验入组的必要生物标志物。

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