前列腺腺癌异常GATA3染色:一个潜在的诊断缺陷。

Timothy M McDonald, Jonathan I Epstein
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引用次数: 5

摘要

鉴别低分化尿路上皮癌和高级别前列腺腺癌是泌尿生殖系统病理学中的一个常见挑战,特别是当肿瘤累及膀胱颈或前列腺尿道时。在临床上,区分这两种肿瘤也很困难。由于这些患者预后和临床管理不同,因此正确诊断至关重要。GATA3被认为是尿路上皮癌的一个敏感和相对特异性的标志物。然而,关于GATA3标记高级别前列腺腺癌的数据很少。本研究的目的是描述前列腺腺癌中具有强烈异常GATA3染色的罕见病例,作为潜在的诊断缺陷。我们在2015年至2020年期间确定了9例GATA3染色异常阳性的前列腺腺癌,作为我们机构大型咨询服务的一部分。9例均为5级组,其中Gleason评分5+5=10者8例,4+5=9者1例。5例来自前列腺,3例来自膀胱,1例来自前列腺尿道。所有的病例在形态学上都是高级别前列腺腺癌的典型,尽管由于诊断不确定而被送去会诊。GATA3阳性强烈,弥漫4例;强,斑片状2例,强,局灶性3例。所有病例NKX3.1阳性,6例p501s阳性,6例PSA阳性,其中7/9例至少表达2种前列腺特异性标志物。目前的研究描述了罕见的前列腺腺癌病例可以显示局灶性或弥漫性强的GATA3染色。为了避免这个诊断陷阱,浸润前列腺、膀胱颈或三角区的未分化癌不仅要用GATA3进行评估,还要用前列腺特异性标志物进行评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aberrant GATA3 Staining in Prostatic Adenocarcinoma: A Potential Diagnostic Pitfall.

Distinguishing between poorly differentiated urothelial carcinoma and high-grade prostatic adenocarcinoma is a common challenge in genitourinary pathology, particularly when the tumor involves the bladder neck or prostatic urethra. Clinically, the distinction between these 2 tumors can also be difficult. Proper diagnosis in these patients is essential as they have differing prognoses and clinical management. GATA3 is thought to be a sensitive and relatively specific marker of urothelial carcinoma. However, there is scant data regarding GATA3 labeling of high-grade prostatic adenocarcinoma. The aim of this study is to describe rare cases with strong aberrant GATA3 staining in prostatic adenocarcinoma as a potential diagnostic pitfall. We identified 9 cases of prostatic adenocarcinoma with aberrant positive GATA3 staining from 2015 to 2020 as part of a large consultation service at our institution. All 9 cases were grade group 5, 8 had a Gleason score of 5+5=10 and 1 had a score of 4+5=9. Five of the cases were from the prostate, 3 from the urinary bladder, and 1 from the prostatic urethra. All cases were morphologically typical of high-grade prostatic adenocarcinoma, although were sent for consultation due to uncertainty in the diagnosis. GATA3 positivity was strong, diffuse in 4 cases; strong, patchy in 2 cases and strong, focal in 3 cases. All cases were positive for NKX3.1, 6 positive for p501s, and 6 positive for PSA, with 7/9 cases showing expression of at least 2 prostate-specific markers. The current study describes that rare cases of prostatic adenocarcinoma can show focal or diffuse strong staining for GATA3. In order to avoid this diagnostic pitfall, undifferentiated carcinomas involving the prostate, bladder neck, or trigone should be evaluated not only with GATA3 but also prostate-specific markers.

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