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Best Practice in Diagnostic Immunohistochemistry: Prostate Carcinoma and Its Mimics in Needle Core Biopsies

机译:免疫组织化学诊断的最佳实践:前列腺癌及其在穿刺针活检中的模拟物

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CONTEXT: The unrelenting challenge encountered when differentiating limited-volume prostate carcinoma and sometimes subtle variants from its many morphologic mimics has increased the use of ancillary immunohistochemistry in routine prostate needle biopsies. The availability of prostate cancer-associated and basal cell-associated markers has been an invaluable addition to diagnostic surgical pathology. OBJECTIVE: To review commonly used immunohistochemical stains, including innovative combinations, for confirmation or differential diagnosis of prostate carcinoma, and to propose appropriately constructed panels using morphologic patterns in prostate needle biopsies. DATA SOURCES: These best practices are based on our experience with routine and consultative case sign-outs and on a review of the published English-language literature from 1987 through 2008. CONCLUSIONS: Basal cell-associated markers p63, high-molecular-weight cytokeratin 34 beta E12, cytokeratin 5/6 or a cocktail containing p63 and high-molecular-weight cytokeratin 34 beta E12 or cytokeratin 5/6 and prostate carcinoma-specific marker alpha-methylacyl coenzyme A (coA) racemase alone or in combination are useful adjuncts in confirming prostatic carcinoma that either lacks diagnostic, qualitative or quantitative features or that has an unusual morphologic pattern (eg, atrophic, pseudohyperplastic) or is in the setting of prior treatment. The combination of alpha-methylacyl coA racemase positivity with negative staining for basal cell-associated markers supports a malignant diagnosis in the appropriate morphologic context. Dual chromogen basal cell- associated markers (p63 [nuclear] and high-molecular-weight cytokeratin 34 beta E12/cytokeratin 5/6 [cytoplasmic]) and alpha-methylacyl coA racemase in an antibody cocktail provide greater sensitivity for the basal cell layer, easing evaluation and minimizing loss of representation of the focal area interest because the staining is performed on one slide. In the posttreatment setting, pancytokeratin facilitates detection of subtle-treated cancer cells. Prostate-specific antigen and prostatic acid phosphatase markers are helpful in excluding secondary malignancies involving the prostate, such as urothelial carcinoma, and occasionally in excluding nonprostatic benign mimickers, such as nephrogenic adenoma, mesonephric gland hyperplasia, and Cowper glands. There is no role for ordering immunohistochemistry prospectively in all cases of prostatic needle biopsies.
机译:背景:区分有限体积的前列腺癌以及有时从其许多形态学模拟中有些微妙的变体时遇到的不懈挑战增加了辅助免疫组织化学在常规前列腺穿刺活检中的应用。前列腺癌相关和基底细胞相关标记的可用性是诊断性手术病理学的宝贵补充。目的:审查常用的免疫组化染色剂,包括创新的组合物,以确认或鉴别诊断前列腺癌,并提出在前列腺穿刺活检中使用形态学模式适当构建的面板。数据来源:这些最佳做法是基于我们在例行和咨询性案例签出方面的经验,以及对1987年至2008年英语文献的评论。结论:基底细胞相关标记物p63,高分子量细胞角蛋白34βE12,细胞角蛋白5/6或含有p63和高分子量细胞角蛋白的混合物34βE12或细胞角蛋白5/6与前列腺癌特异性标志物α-甲基酰基辅酶A(coA)消旋酶单独或组合使用是有用的辅助剂确认缺乏诊断,定性或定量特征或具有异常形态特征(例如萎缩性,假性增生性)或正在接受治疗的前列腺癌。 α-甲基酰基辅酶A消旋酶阳性与基础细胞相关标记阴性染色相结合,可在适当的形态学背景下进行恶性诊断。抗体混合物中的双色原基细胞相关标记(p63 [核]和高分子量细胞角蛋白34 beta E12 /细胞角蛋白5/6 [细胞质])和α-甲基酰基辅酶A外消旋酶为基底细胞层提供了更高的敏感性,由于染色是在一张载玻片上进行的,因此可以简化评估并最大程度地减少对焦点区域关注的表示损失。在后处理环境中,全细胞角蛋白有助于检测经微处理的癌细胞。前列腺特异性抗原和前列腺酸磷酸酶标志物有助于排除涉及前列腺的继发性恶性肿瘤,例如尿路上皮癌,偶尔还有助于排除非前列腺良性模仿者,例如肾源性腺瘤,中肾增生和考珀氏腺。在所有前列腺穿刺活检病例中,没有前瞻性地命令免疫组化的作用。

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    《Archives of Pathology & Laboratory Medicine》 |2008年第9期|p.1388-1396|共9页
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    Gladell P. Paner, MD, Daniel J. Luthringer, MD, Mahul B. Amin, MDAccepted for publication May 16, 2008.From the Department of Pathology and Laboratory Medicine, Cedars- Sinai Medical Center, Los Angeles, Calif. Dr Paner is now located at Loyola University Medical Center, Maywood, Ill.The authors have no relevant financial interest in the products or companies described in this article.This article is provided for educational purposes only and is not intended to suggest either a practice standard or the only acceptable pathway for diagnostic evaluation. The views presented reflect the authors' opinions. The application of these opinions to a particular medical situation must be guided by the informed medical judgment of the responsible pathologist(s) based on the individual circumstances presented by the patient. The College of American Pathologists has no responsibility for the content or application of the views expressed herein.Reprints: Mahul B. Amin, MD, Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, 8700 Beverly Blvd, Suite 8728, Los Angeles, CA 90048 (e-mail: aminm@cshs.org).,;

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