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具有重叠组织学特征的黏液性管状和梭形细胞癌与乳头状肾细胞癌的独特基因组拷贝数改变。

Distinct Genomic Copy Number Alterations Distinguish Mucinous Tubular and Spindle Cell Carcinoma of the Kidney From Papillary Renal Cell Carcinoma With Overlapping Histologic Features.

机构信息

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.

出版信息

Am J Surg Pathol. 2018 Jun;42(6):767-777. doi: 10.1097/PAS.0000000000001038.

Abstract

Mucinous tubular and spindle cell carcinoma (MTSCC) of the kidney is a rare type of renal cell carcinoma that frequently exhibits histologic and immunophenotypic features overlapping with type 1 papillary renal cell carcinoma (PRCC). To clarify molecular attributes that can be used for this difficult differential diagnosis, we sought to delineate the genome-wide copy number alterations in tumors displaying classic histologic features of MTSCC in comparison to the solid variant of type 1 PRCC and indeterminate cases with overlapping histologic features. The study included 11 histologically typical MTSCC, 9 tumors with overlapping features between MTSCC and PRCC, and 6 cases of solid variant of type 1 PRCC. DNA samples extracted from macrodissected or microdissected tumor areas were analyzed for genome-wide copy number alterations using an SNP-array platform suitable for clinical archival material. All cases in the MTSCC group exhibited multiple chromosomal losses, most frequently involving chromosomes 1, 4, 6, 8, 9, 13, 14, 15, and 22, while lacking trisomy 7 or 17. In contrast, cases with overlapping morphologic features of MTSCC and PRCC predominantly showed multiple chromosomal gains, most frequently involving chromosomes 7, 16, 17, and 20, similar to the chromosomal alteration pattern that was seen in the solid variant of type 1 PRCC cases. Morphologic comparison of these molecularly characterized tumors identified histologic features that help to distinguish MTSCC from PRCC, but immunohistochemical profiles of these tumors remained overlapping, including a marker for Hippo-Yes-associated protein signaling. Characteristic patterns of genome-wide copy number alterations strongly support MTSCC and PRCC as distinct entities despite their immunohistochemical and certain morphologic overlap, and help define histologic features useful for the classification of questionable cases.

摘要

肾黏液性管状和梭形细胞癌(MTSCC)是一种罕见的肾细胞癌,其组织学和免疫表型特征常与 1 型乳头状肾细胞癌(PRCC)重叠。为了阐明可用于这种困难的鉴别诊断的分子特征,我们试图描绘显示经典 MTSCC 组织学特征的肿瘤与 1 型 PRCC 的实性变体和具有重叠组织学特征的不确定病例的全基因组拷贝数改变。该研究包括 11 例组织学典型的 MTSCC、9 例 MTSCC 和 PRCC 之间具有重叠特征的肿瘤以及 6 例 1 型 PRCC 的实性变体。从宏观或微观解剖肿瘤区域提取的 DNA 样本,使用适合临床存档材料的 SNP 阵列平台进行全基因组拷贝数改变分析。MTSCC 组中的所有病例均表现出多个染色体缺失,最常涉及染色体 1、4、6、8、9、13、14、15 和 22,而缺乏三体 7 或 17。相比之下,具有 MTSCC 和 PRCC 重叠形态特征的病例主要表现出多个染色体获得,最常涉及染色体 7、16、17 和 20,与 1 型 PRCC 实性变体病例中观察到的染色体改变模式相似。对这些分子特征肿瘤的形态学比较确定了有助于将 MTSCC 与 PRCC 区分开来的组织学特征,但这些肿瘤的免疫组织化学特征仍然重叠,包括 Hippo-Yes 相关蛋白信号的标志物。全基因组拷贝数改变的特征模式强烈支持 MTSCC 和 PRCC 是不同的实体,尽管它们具有免疫组织化学和某些形态学重叠,并有助于定义有助于分类可疑病例的组织学特征。

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