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具有YAP1融合的多孔性附属器皮肤肿瘤表现出相似的组织病理学特征:一组6例YAP1重排的附属器皮肤肿瘤。

Poroid adnexal skin tumors with YAP1 fusions exhibit similar histopathologic features: A series of six YAP1-rearranged adnexal skin tumors.

作者信息

Prieto-Granada Carlos, Morlote Diana, Pavlidakey Peter, Rodriguez-Waitkus Paul, Ramirez Cristina, Florento Elena, Swensen Jeffrey, Gatalica Zoran, Stevens Todd M

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Department of Dermatology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

J Cutan Pathol. 2021 Sep;48(9):1139-1149. doi: 10.1111/cup.14008. Epub 2021 Mar 21.

Abstract

BACKGROUND

Adnexal skin tumors are diagnostically challenging with few known molecular signatures. Recently, however, YAP1-MAML2 and YAP1-NUTM1 fusions were identified in poroid adnexal skin tumors.

METHODS

Herein, we subjected eight poroid adnexal skin tumors (three poromas and five porocarcinomas) to fusion gene analysis by whole transcriptome sequencing and next-generation DNA sequencing analysis.

RESULTS

YAP1 fusions were identified in six cases. YAP1-NUTM1 fusions were identified in two poromas and three porocarcinomas. A single case of porocarcinoma harbored a YAP1-MAML2 fusion. Two cases were negative for gene fusion. All cases that harbored YAP1-NUTM1 fusions showed nuclear protein in testis (NUT) expression by immunohistochemistry, with NUT being negative in the YAP1-MAML2-positive case. In this case series, we provide a detailed histopathologic description of six YAP1-fused poroid skin tumors, which we show harbor reproducible histopathologic features, to include broad, bulbous tumor tongues with admixtures of basaloid, poroid cells punctuated by squamatized cuticles and ductules, with uniform tumor nuclei featuring frequent grooves and pseudonuclear inclusions.

CONCLUSIONS

Awareness of the characteristic histopathologic features of YAP1-fused poroid adnexal skin tumor is a step toward a more reproducible classification of adnexal skin tumors as well as a step toward targeted therapy for metastatic and/or unresectable examples of this poroid group of neoplasms.

摘要

背景

附件皮肤肿瘤的诊断具有挑战性,已知的分子特征很少。然而,最近在类汗孔瘤性附件皮肤肿瘤中发现了YAP1-MAML2和YAP1-NUTM1融合基因。

方法

在此,我们通过全转录组测序和二代DNA测序分析,对8例类汗孔瘤性附件皮肤肿瘤(3例汗孔瘤和5例汗孔癌)进行融合基因分析。

结果

6例中鉴定出YAP1融合基因。在2例汗孔瘤和3例汗孔癌中鉴定出YAP1-NUTM1融合基因。1例汗孔癌存在YAP1-MAML2融合基因。2例基因融合检测为阴性。所有存在YAP1-NUTM1融合基因的病例免疫组化显示睾丸核蛋白(NUT)表达阳性,而YAP1-MAML2阳性病例中NUT为阴性。在这个病例系列中,我们对6例YAP1融合的类汗孔瘤性皮肤肿瘤进行了详细的组织病理学描述,显示其具有可重复的组织病理学特征,包括宽而圆的肿瘤舌,伴有基底样、类汗孔样细胞混合,有角化的角质层和小导管,肿瘤细胞核均匀,有频繁的沟和假核内包涵体。

结论

认识YAP1融合的类汗孔瘤性附件皮肤肿瘤的特征性组织病理学特征,是朝着更可重复的附件皮肤肿瘤分类迈出的一步,也是朝着对这类类汗孔瘤性肿瘤的转移性和/或不可切除病例进行靶向治疗迈出的一步。

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