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SMARCA4 缺陷型未分化子宫肉瘤(子宫恶性横纹肌样瘤):一种与未分化癌不同的临床病理实体。

SMARCA4-deficient undifferentiated uterine sarcoma (malignant rhabdoid tumor of the uterus): a clinicopathologic entity distinct from undifferentiated carcinoma.

机构信息

Division of Women's and Perinatal Pathology, Department of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.

Department of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.

出版信息

Mod Pathol. 2018 Sep;31(9):1442-1456. doi: 10.1038/s41379-018-0049-z. Epub 2018 Apr 26.

Abstract

Small cell carcinoma of the ovary, hypercalcemic type is a rare, aggressive malignancy which usually occurs in young women and is characterized by mutations in SMARCA4, with few other alterations. We recently encountered uterine tumors with morphologic, immunohistochemical, and genetic similarities to small cell carcinoma of the ovary, hypercalcemic type. Herein we report the clinicopathologic and molecular features (using a targeted massively parallel sequencing [MPS] assay) of these tumors. The cases were diagnosed on cervical and endometrial biopsies (n = 2, 34, and 29 years) or hysterectomy and bilateral salpingo-oophorectomy (n = 3, 25, 33, and 58 years). The tumors were composed of sheets of large atypical epithelioid cells with prominent rhabdoid morphology, indistinguishable from the "large cell" variant of small cell carcinoma of the ovary, hypercalcemic type. In three cases, the ovaries were pathologically examined to exclude a primary ovarian malignancy. Immunohistochemically, four of four cases showed SMARCA4 loss, and were negative or only focally positive for keratins, EMA, and claudin-4. One of three cases was positive for WT-1. Targeted MPS was successfully performed on 4 of 5 tumors, and showed recurrent mutations in SMARCA4, with few other alterations. Of the cases diagnosed on hysterectomy, all had extensive lymphovascular invasion, extra-uterine spread, and marked infiltrative growth. These tumors were uniformly aggressive; all patients died of disease (median survival 7 months, range 1-43 months). We propose this entity be called "SMARCA4-deficient undifferentiated uterine sarcoma (malignant rhabdoid tumor of the uterus)", a term which describes both the tumor's underlying molecular abnormality and its morphology. Its unique clinicopathologic and molecular features differentiate it from other related malignancies, including undifferentiated endometrial carcinoma, small cell carcinoma of the ovary (hypercalcemic type), and epithelioid sarcoma. We review and discuss previously reported "rhabdoid tumors of the uterus;" while they are a heterogenous group of tumors, some of them are likely examples of this entity. Correctly identifying cases of SMARCA4-deficient uterine sarcoma from histologic mimics is important as it may have prognostic, predictive, and germline implications.

摘要

卵巢小细胞癌,高钙血症型是一种罕见的侵袭性恶性肿瘤,通常发生在年轻女性中,其特征是 SMARCA4 突变,其他改变较少。我们最近遇到了一些具有与卵巢小细胞癌,高钙血症型相似形态学、免疫组织化学和遗传学特征的子宫肿瘤。在此,我们报告这些肿瘤的临床病理和分子特征(使用靶向大规模平行测序 [MPS] 检测)。这些病例分别通过宫颈和子宫内膜活检(n=2、34 和 29 岁)或子宫切除术和双侧输卵管卵巢切除术(n=3、25、33 和 58 岁)诊断。肿瘤由大片大异型上皮样细胞组成,具有明显的横纹肌样形态,与卵巢小细胞癌,高钙血症型的“大细胞”变体无法区分。在三个病例中,对卵巢进行了病理检查以排除原发性卵巢恶性肿瘤。免疫组织化学染色显示,4 例中有 4 例 SMARCA4 缺失,并且对角蛋白、EMA 和 Claudin-4 呈阴性或仅局灶阳性。3 例中有 1 例 WT-1 阳性。对 5 例肿瘤中的 4 例成功进行了靶向 MPS,显示出 SMARCA4 反复突变,其他改变较少。在子宫切除术诊断的病例中,所有病例均有广泛的淋巴血管侵犯、宫外扩散和明显的浸润性生长。这些肿瘤均具有侵袭性;所有患者均因疾病死亡(中位生存时间 7 个月,范围 1-43 个月)。我们建议将该实体命名为“SMARCA4 缺失未分化子宫肉瘤(子宫恶性横纹肌样瘤)”,该术语既描述了肿瘤的潜在分子异常,也描述了其形态。其独特的临床病理和分子特征使其与其他相关恶性肿瘤区分开来,包括未分化子宫内膜癌、卵巢小细胞癌(高钙血症型)和上皮样肉瘤。我们回顾并讨论了以前报道的“子宫横纹肌样瘤”;虽然它们是一组异质性肿瘤,但其中一些可能是该实体的例子。正确识别 SMARCA4 缺失性子宫肉瘤与组织学模拟物之间的关系非常重要,因为它可能具有预后、预测和种系意义。

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