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一系列原发性肾 CIC 重排肉瘤的临床病理特征及全面分子分析。

Clinicopathologic Features of a Series of Primary Renal CIC-rearranged Sarcomas With Comprehensive Molecular Analysis.

机构信息

Alpert Medical School of Brown University, Rhode Island Hospital, Providence, RI.

Children's of Alabama & University of Alabama Medical School, Birmingham, AL.

出版信息

Am J Surg Pathol. 2018 Oct;42(10):1360-1369. doi: 10.1097/PAS.0000000000001098.

Abstract

CIC-rearranged sarcomas rarely occur in visceral organs including the kidney. The most common fusion partner with CIC is the DUX4 gene, but variant fusion partners have also been reported. Herein, we describe the clinicopathologic features and comprehensive molecular profiling of 4 cases of primary renal CIC-rearranged sarcomas. All cases occurred in females, age range 13 to 82 years and included 3 resections and 1 needle biopsy specimen. There was a tendency for development of metastatic disease predominantly to the lungs and poor disease outcome despite different treatment strategies. Histologically, variable round cell (20% to 100%), spindle cell (0% to 80%), and rhabdoid morphologies (0% to 20%) were seen. By immunohistochemistry diffuse WT1 nuclear (2 to 3+, ∼90%) labeling was present in 1 case, with cytoplasmic staining in the others (3+, 40% to 75%). CD99 was focally positive in all 4 cases (≤10%); 1 case each was diffusely positive for c-myc (2 to 3+, ∼90%) and ETV4 (3+, ∼90%); 1 case was focally positive for c-myc (2+, ∼5%) and calretinin (2+, ∼5%); and all cases were negative for cytokeratin and NKX2.2. CIC rearrangement by fluorescence in situ hybridization was present in the 3 cases tested. Comprehensive genomic profiling (CGP) of 3 cases revealed a CIC-DUX4 fusion in 2 cases, and 1 CIC-NUTM1 fusion. All 4 CIC-rearranged renal sarcomas had low mutation burden, and except HLA-A and MLL mutations lacked genomic alterations in other oncogenic drivers. Material from the needle biopsy was insufficient for CGP but that case was positive with the DUX4 immunohistochemical stain as were the 2 CIC-DUX4 tumors. In conclusion, CIC-rearranged sarcomas rarely occur in the kidney with a tendency for poor outcome and in this series we illustrate an example with CIC-NUTM1 fusion, an emerging variant, at a visceral site. Testing by fluorescence in situ hybridization or CGP is optimal to avoid missing cases that harbor variant fusion partners.

摘要

CIC 重排肉瘤很少发生于内脏器官,包括肾脏。与 CIC 最常见的融合伙伴是 DUX4 基因,但也有报道称存在变异融合伙伴。在此,我们描述了 4 例原发性肾脏 CIC 重排肉瘤的临床病理特征和全面的分子特征。所有病例均发生于女性,年龄 13 至 82 岁,包括 3 例切除术和 1 例针吸活检标本。尽管采用了不同的治疗策略,这些病例主要表现为转移性疾病,且预后不良。组织学上,可见各种形态的小圆细胞(20%至 100%)、梭形细胞(0%至 80%)和横纹肌样形态(0%至 20%)。免疫组化显示,1 例弥漫性 WT1 核阳性(2 至 3+,约 90%),其余 3 例细胞质染色阳性(3+,40%至 75%)。4 例均局灶性 CD99 阳性(≤10%);各有 1 例弥漫性 c-myc(2 至 3+,约 90%)和 ETV4(3+,约 90%)阳性;1 例局灶性 c-myc(2+,约 5%)和钙视网膜蛋白(2+,约 5%)阳性;所有病例均阴性 CK 和 NKX2.2。3 例经荧光原位杂交检测到 CIC 重排。3 例进行了全面基因组分析(CGP),其中 2 例为 CIC-DUX4 融合,1 例为 CIC-NUTM1 融合。4 例 CIC 重排肾肉瘤均具有低突变负担,除 HLA-A 和 MLL 突变外,其他致癌驱动基因均无基因组改变。针吸活检的组织不足以进行 CGP,但该病例与 2 例 CIC-DUX4 肿瘤一样,免疫组化 DUX4 染色阳性。总之,CIC 重排肉瘤很少发生于肾脏,预后不良,本系列中我们展示了一例内脏部位 CIC-NUTM1 融合的病例,这是一种新兴的变异融合。通过荧光原位杂交或 CGP 检测是避免遗漏具有变异融合伙伴的最佳方法。

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