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免疫组织化学染色在皮肤病理中的应用。

Immunohistochemistry for PRAME in Dermatopathology.

机构信息

Pathologist, Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Pathologist, Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY; and.

出版信息

Am J Dermatopathol. 2023 Nov 1;45(11):733-747. doi: 10.1097/DAD.0000000000002440.

DOI:10.1097/DAD.0000000000002440
PMID:37856737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10593485/
Abstract

Preferentially expressed antigen in melanoma (PRAME) is a tumor-associated antigen first identified in a melanoma patient and found to be expressed in most melanomas as well as in variable levels in other malignant neoplasms of epithelial, mesenchymal, or hematolymphoid lineage. Detection of PRAME expression in formalin-fixed paraffin-embedded tissue is possible by immunohistochemistry (IHC) with commercially available monoclonal antibodies. In situ and invasive melanoma frequently show a diffuse pattern of nuclear PRAME immunoreactivity which contrasts with the infrequent and typically nondiffuse staining seen in nevi. In many challenging melanocytic tumors, results of PRAME IHC and other ancillary tests correlate well, but not always: The tests are not interchangeable. Most metastatic melanomas are positive for PRAME, whereas nodal nevi are not. Numerous studies on PRAME IHC have become available in the past few years with results supporting the value of PRAME IHC as an ancillary tool in the evaluation of melanocytic lesions and providing insights into limitations in sensitivity and specificity as well as possible pitfalls that need to be kept in mind by practicing pathologists.

摘要

黑色素瘤中优先表达的抗原(PRAME)是一种肿瘤相关抗原,最初在一名黑色素瘤患者中被发现,发现在大多数黑色素瘤中均有表达,并且在其他上皮、间充质或造血淋巴谱系的恶性肿瘤中也以不同水平表达。通过免疫组织化学(IHC)用商业上可获得的单克隆抗体,可以检测福尔马林固定石蜡包埋组织中 PRAME 的表达。原位和侵袭性黑色素瘤通常显示弥漫性核 PRAME 免疫反应性,与痣中罕见且通常非弥漫性染色形成对比。在许多具有挑战性的黑色素瘤中,PRAME IHC 和其他辅助检测的结果相关性良好,但并非总是如此:这些检测不可互换。大多数转移性黑色素瘤对 PRAME 呈阳性,而结内痣则不是。过去几年,关于 PRAME IHC 的研究已经很多,结果支持 PRAME IHC 作为评估黑色素细胞病变的辅助工具的价值,并提供了对敏感性和特异性的局限性以及需要由实践病理学家注意的可能陷阱的深入了解。

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Cutaneous melanoma.皮肤黑色素瘤

本文引用的文献

1
PRAME Staining in Sinonasal Mucosal Melanoma: A Single-Center Experience.PRAME 染色在鼻腔鼻窦黏膜黑色素瘤中的应用:单中心经验。
Head Neck Pathol. 2023 Jun;17(2):401-408. doi: 10.1007/s12105-022-01515-9. Epub 2022 Dec 31.
2
PRAME Immuno-Expression in Cutaneous Sebaceous Carcinoma: A Single Institutional Experience.PRAME在皮肤皮脂腺癌中的免疫表达:单机构经验
J Clin Med. 2022 Nov 24;11(23):6936. doi: 10.3390/jcm11236936.
3
Performance of PRAME immunohistochemistry compared with that of c-Kit, c-Myc, or cyclin D1 for the diagnosis of acral melanocytic tumors.
Nat Rev Dis Primers. 2025 Apr 3;11(1):23. doi: 10.1038/s41572-025-00603-8.
4
The Utilization of PRAME in the Diagnosis, Prognosis, and Treatment of Melanoma.PRAME 在黑色素瘤的诊断、预后和治疗中的应用。
Cells. 2024 Oct 20;13(20):1740. doi: 10.3390/cells13201740.
5
Utilizing PRAME Expression and a Meta-Analytic Framework for iSALT to Explore Atypical Late-Onset Nevi of the Elderly and Their Relationship With Lentiginous and Nested Nevoid Melanomas.利用PRAME表达和iSALT的荟萃分析框架来探索老年人非典型迟发性痣及其与雀斑样和巢状痣样黑色素瘤的关系。
Am J Dermatopathol. 2024 Dec 1;46(12):825-832. doi: 10.1097/DAD.0000000000002847. Epub 2024 Oct 15.
6
A Narrative Review of the Evolution of Diagnostic Techniques and Treatment Strategies for Acral Lentiginous Melanoma.肢端雀斑样黑素瘤的诊断技术和治疗策略的演变:叙述性回顾。
Int J Mol Sci. 2024 Sep 27;25(19):10414. doi: 10.3390/ijms251910414.
7
Appropriate Statistical Methods to Assess Cross-study Diagnostic 23-Gene Expression Profile Test Performance for Cutaneous Melanocytic Neoplasms.评估皮肤黑素细胞肿瘤跨研究诊断 23 基因表达谱检测性能的适当统计方法。
Am J Dermatopathol. 2024 Dec 1;46(12):833-838. doi: 10.1097/DAD.0000000000002808. Epub 2024 Aug 14.
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bioRxiv. 2024 Jul 26:2024.07.26.605293. doi: 10.1101/2024.07.26.605293.
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Histopathology. 2023 Jan;82(2):285-295. doi: 10.1111/his.14814. Epub 2022 Oct 13.
9
PRAME Immunoexpression in 275 Cutaneous Melanocytic Lesions: A Double Institutional Experience.275例皮肤黑素细胞性病变中PRAME的免疫表达:一项双机构研究经验
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Histopathology. 2022 Dec;81(6):818-825. doi: 10.1111/his.14797. Epub 2022 Sep 28.