伴有体细胞 BRCA2 突变的侵袭性肾细胞癌--一种新出现的实体?病例报告与文献综述。

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-12-14 DOI:10.1007/s00428-024-04008-y
Jung Woo Kwon, Priscilla Louise Natcher, Tatjana Antic
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引用次数: 0

摘要

BRCA2 基因突变在肾肿瘤发生中的作用在很大程度上仍不明确。目前仅有两例 BRCA2 基因突变的肾细胞癌(RCC)病例报告,这两例病例均为高级别 RCC,具有不同的结构形态,包括管状和实性。据描述,肿瘤细胞具有嗜酸性细胞质和突出的核小体。本研究描述了另一例伴有体细胞BRCA2突变的高级别RCC病例,该病例具有不同的结构模式,肿瘤细胞具有嗜酸性细胞质和突出的核小体。免疫组化染色显示 PAX8、CAIX、CD10、CK7、CK20 和 P504S 共同表达。在 RCC 的检查过程中,这种不寻常的常用 IHC 染色的共同表达可能是一个潜在的诊断陷阱。尽管这种病例非常罕见,但由于其临床表现具有侵袭性、存在种系突变的可能性以及目前对 BRCA2 突变肿瘤的治疗方案,病理学家有必要了解这种形式的 RCC。
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Aggressive renal cell carcinoma with somatic BRCA2 mutation-an emerging entity? A case report with literature review.

Role of BRCA2 gene mutation in renal tumorigenesis remains largely unclear. There are only two case reports of renal cell carcinoma (RCC) with BRCA2 mutation, both of which showed a high-grade RCC with various architectural patterns including tubulopapillary and solid. The tumor cells were described as having eosinophilic cytoplasm and prominent nucleoli. The current study describes another case of high-grade RCC with somatic BRCA2 mutation with various architectural patterns and cells with eosinophilic cytoplasm and prominent nucleoli. Immunohistochemical staining showed co-expression of PAX8, CAIX, CD10, CK7, CK20, and P504S. This unusual co-expression of the commonly used IHC stains during the workup of RCC could serve as a potential diagnostic pitfall. Although very rare, it is important for pathologists to be aware of this form of RCC due to its aggressive clinical behavior, possibility of a germline mutation, and current therapeutic options for tumors with BRCA2 mutation.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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