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PRAME immunohistochemistry for melanoma diagnosis: A STARD-compliant diagnostic accuracy study.PRAME 免疫组化在黑色素瘤诊断中的应用:一项符合 STARD 标准的诊断准确性研究。
J Cutan Pathol. 2022 Sep;49(9):780-786. doi: 10.1111/cup.14267. Epub 2022 Jun 28.
2
PRAME Expression Correlates With Genomic Aberration and Malignant Diagnosis of Spitzoid Melanocytic Neoplasms.PRAME 表达与 Spitz 样黑色素细胞肿瘤的基因组改变和恶性诊断相关。
Am J Dermatopathol. 2022 Aug 1;44(8):575-580. doi: 10.1097/DAD.0000000000002208. Epub 2022 Apr 27.
3
PRAME immunohistochemistry of spitzoid neoplasms.棘皮瘤样肿瘤的 PRAME 免疫组化染色。
J Cutan Pathol. 2022 Aug;49(8):709-716. doi: 10.1111/cup.14245. Epub 2022 May 24.
4
Dermatopathologist Perceptions of Overdiagnosis of Melanocytic Skin Lesions and Association With Diagnostic Behaviors.皮肤科病理学家对黑素细胞性皮肤病变过度诊断的看法及其与诊断行为的关联。
JAMA Dermatol. 2022 Jun 1;158(6):675-679. doi: 10.1001/jamadermatol.2022.0489.
5
Estimating Overdiagnosis of Melanoma Using Trends Among Black and White Patients in the US.使用美国黑人和白人患者的趋势估计黑色素瘤的过度诊断。
JAMA Dermatol. 2022 Apr 1;158(4):426-431. doi: 10.1001/jamadermatol.2022.0139.
6
Are Specific Body Sites Prone for Wound Infection After Skin Surgery? A Systematic Review and Meta-Analysis.皮肤手术后,特定部位是否容易发生伤口感染?系统评价和荟萃分析。
Dermatol Surg. 2022 Apr 1;48(4):406-410. doi: 10.1097/DSS.0000000000003387.
7
Immunohistochemistry in melanocytic lesions: Updates with a practical review for pathologists.黑素细胞性病变的免疫组织化学:为病理学家提供的实用综述及更新
Semin Diagn Pathol. 2022 Jul;39(4):239-247. doi: 10.1053/j.semdp.2021.12.003. Epub 2022 Jan 1.
8
Shared Gene Expression and Immune Pathway Changes Associated with Progression from Nevi to Melanoma.与痣进展为黑色素瘤相关的共享基因表达和免疫通路变化
Cancers (Basel). 2021 Dec 21;14(1):3. doi: 10.3390/cancers14010003.
9
PRAME Expression in Challenging Dermal Melanocytic Neoplasms and Soft Tissue Tumors With Melanocytic Differentiation.PRAME 在具有黑色素细胞分化的具有挑战性的皮肤黑色素细胞肿瘤和软组织肿瘤中的表达。
Am J Dermatopathol. 2022 Jun 1;44(6):404-410. doi: 10.1097/DAD.0000000000002128. Epub 2022 Jan 5.
10
Preferentially expressed Antigen in MElanoma immunohistochemistry as an adjunct for evaluating ambiguous melanocytic proliferation.黑色素瘤中优先表达抗原的免疫组织化学检测作为评估不明确黑素细胞增殖的辅助手段
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皮肤黑素细胞肿瘤基因表达谱辅助诊断检测使用的医师指南

A Physician's Guide to the Use of Gene Expression Profile Ancillary Diagnostic Testing for Cutaneous Melanocytic Neoplasms.

作者信息

Marks Etan, Jarell Abel, Ludzik Joanna, Farberg Aaron S, Rabinovitz Harold S, Phelps Robert G, Cockerell Clay J, Witkowski Alexander

机构信息

Dr. Marks is with Dermatopathology, Kansas City University-Graduate Medical Education Consortium in Oviedo, Florida, and Advanced Dermatology and Cosmetic Surgery in Oviedo, Florida.

Dr. Jarell is with Granite State Dermatology, PC in Portsmouth, New Hampshire.

出版信息

J Clin Aesthet Dermatol. 2023 Apr;16(4):12-20.

PMID:37077930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10110288/
Abstract

OBJECTIVES

Some melanocytic neoplasms suspicious for melanoma require additional workup to arrive at a final diagnosis. Within the last eight years, gene expression profiling (GEP) has become an important ancillary tool to aid in the diagnosis of melanocytic neoplasms with uncertain malignant potential. As the usage of two commercially available tests (23-GEP and 35-GEP) evolves, it is important to answer key questions about optimal utilization and their impact on patient care.

METHODS

Recent and relevant articles answering the following questions were included in the review. First, how do dermatopathologists synthesize the available literature, the latest guidelines, and their clinical experience to determine which cases would be most likely to benefit from GEP testing? Second, how best can a dermatologist convey to their dermatopathologist that the use of GEP in the diagnostic process could provide a more clearly defined result and thereby help empower the dermatologist to provide higher-quality patient care when making specific patient management decisions for otherwise pathologically ambiguous lesions?

RESULTS

When interpreted in the context of the clinical, pathologic, and laboratory information, GEP results can facilitate the rendering of timely, accurate, and definitive diagnoses for melanocytic lesions with otherwise uncertain malignant potential to inform personalized treatment and management plans.

LIMITATIONS

This was a narrative review focused on clinical use of GEP compared to other ancillary diagnostic tests performed postbiopsy.

CONCLUSION

Open communication between dermatopathologists and dermatologists, especially regarding GEP testing, can be a vital component to achieve appropriate clinicopathologic correlation for otherwise ambiguous melanocytic lesions.

摘要

目的

一些疑似黑色素瘤的黑素细胞肿瘤需要进一步检查以得出最终诊断。在过去八年中,基因表达谱分析(GEP)已成为辅助诊断具有不确定恶性潜能的黑素细胞肿瘤的重要工具。随着两种市售检测方法(23-GEP和35-GEP)的应用不断发展,回答有关最佳利用及其对患者护理影响的关键问题非常重要。

方法

本次综述纳入了近期回答以下问题的相关文章。第一,皮肤病理学家如何综合现有文献、最新指南及其临床经验,以确定哪些病例最有可能从GEP检测中获益?第二,皮肤科医生如何最好地向其皮肤病理学家传达,在诊断过程中使用GEP可以提供更明确的结果,从而帮助皮肤科医生在对其他病理情况不明确的病变做出具体患者管理决策时,提供更高质量的患者护理?

结果

在临床、病理和实验室信息的背景下进行解读时,GEP结果有助于对具有不确定恶性潜能的黑素细胞病变及时、准确地做出明确诊断,从而为个性化治疗和管理计划提供依据。

局限性

这是一项叙述性综述,重点关注与活检后进行的其他辅助诊断测试相比,GEP的临床应用。

结论

皮肤病理学家和皮肤科医生之间的开放沟通,尤其是关于GEP检测的沟通,可能是对其他不明确的黑素细胞病变实现适当临床病理相关性的重要组成部分。