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雄激素剥夺治疗后继发的转移性鳞状细胞癌:附临床病理和分子特征的病例报告。

Metastatic squamous cell carcinoma transformed from prostatic adenocarcinoma following androgen deprivation therapy: A case report with clinicopathologic and molecular findings.

机构信息

VA Palo Alto Health Care System, Pathology and Laboratory Service, Palo Alto, California, USA.

出版信息

Diagn Cytopathol. 2020 Dec;48(12):E14-E17. doi: 10.1002/dc.24539. Epub 2020 Jul 6.

Abstract

Squamous cell carcinoma (SCC) of the prostate is a rare and clinically aggressive entity that may arise de novo or through transformation of prostatic adenocarcinoma, typically following hormonal or radiation therapy. Confirmation of prostatic origin, especially when evaluating a metastatic focus, often requires correlation with clinical and imaging findings, as the morphologic and immunohistochemical features of SCC are not organ-specific. Comprehensive genomic profiling (CGP) may provide additional information useful for confirming the primary site and for identifying potential targeted therapy options. CGP data may also contribute to our understanding of the molecular basis of squamous differentiation in prostatic malignancies. However, these data are limited, and to our knowledge, there are only three previously published cases of prostatic SCC with reported CGP findings. Herein, we report a case of metastatic keratinizing SCC diagnosed by core needle biopsy in a 68-year-old man with a history of prostatic adenocarcinoma status post radical prostatectomy and androgen deprivation therapy (ADT). NKX3.1 immunohistochemistry was negative. CGP was performed, and a TMPRSS2-ERG fusion, among other genetic alterations, was detected, supporting a diagnosis of metastatic SCC transformed from prostatic adenocarcinoma following ADT. This case supports the use of CGP or other molecular techniques not only to query potential targeted therapy options but also to refine the diagnosis and confirm the primary site of disease in cases with non-specific morphologic and immunophenotypic features, such as SCC.

摘要

前列腺鳞状细胞癌(SCC)是一种罕见且具有临床侵袭性的实体瘤,可能是从头发生长,也可能是在激素或放射治疗后由前列腺腺癌转化而来。为了确认前列腺的起源,特别是在评估转移性病灶时,通常需要与临床和影像学发现相关联,因为 SCC 的形态和免疫组织化学特征不是器官特异性的。全面基因组分析(CGP)可能提供有助于确认原发部位和确定潜在靶向治疗选择的额外信息。CGP 数据还可能有助于我们了解前列腺恶性肿瘤中鳞状分化的分子基础。然而,这些数据是有限的,据我们所知,只有三例先前发表的前列腺 SCC 病例报告了 CGP 结果。本文报告了一例转移性角化 SCC 病例,该患者为 68 岁男性,有前列腺腺癌根治性前列腺切除术和雄激素剥夺治疗(ADT)病史。NKX3.1 免疫组化呈阴性。进行了 CGP,检测到 TMPRSS2-ERG 融合等遗传改变,支持 ADT 后由前列腺腺癌转化而来的转移性 SCC 的诊断。该病例支持使用 CGP 或其他分子技术,不仅可以查询潜在的靶向治疗选择,还可以在形态学和免疫表型特征不明确的情况下(如 SCC),用于细化诊断并确认疾病的原发部位。

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