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卵巢小细胞癌,高钙血症型:一名青少年双侧病例报告及与SMARCA4种系突变的相关性

Small Cell Carcinoma of the Ovary, Hypercalcemic Type: Report of a Bilateral Case in a Teenager Associated with SMARCA4 Germline Mutation.

作者信息

Lavrut Pierre-Marie, Le Loarer François, Normand Charline, Grosos Céline, Dubois Rémi, Buenerd Annie, Conter Cécile, Dijoud Frédérique, Blay Jean-Yves, Collardeau-Frachon Sophie

机构信息

1 Department of Pathology, Hôpital Femme Mère Enfant, CHU de Lyon, France.

2 Department of Biopathology, Centre Léon Bérard, Lyon, France.

出版信息

Pediatr Dev Pathol. 2016 Jan-Feb;19(1):56-60. doi: 10.2350/15-04-1624-CR.1. Epub 2015 Jul 31.

Abstract

Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT), is a highly aggressive neoplasm that typically occurs in young females. Paraneoplastic hypercalcemia is associated in two thirds of the cases. Recent studies demonstrated that this rare tumor harbors the same molecular features of malignant rhabdoid tumor secondary to SMARCA4/BRG1 mutations. We illustrate herein a typical bilateral case of SCCOHT with comprehensive molecular characterization in a 14-year-old girl. We also discuss the value of SMARCA4 immunostaining in the diagnostic approach of undifferentiated ovarian and pelvic malignancies.

摘要

卵巢高钙血症型小细胞癌(SCCOHT)是一种侵袭性很强的肿瘤,通常发生于年轻女性。三分之二的病例伴有副肿瘤性高钙血症。最近的研究表明,这种罕见肿瘤具有与继发于SMARCA4/BRG1突变的恶性横纹肌样瘤相同的分子特征。本文展示了一名14岁女孩的典型双侧SCCOHT病例,并进行了全面的分子特征分析。我们还讨论了SMARCA4免疫染色在未分化卵巢和盆腔恶性肿瘤诊断方法中的价值。

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