Marks Etan, Jarell Abel, Ludzik Joanna, Farberg Aaron S, Rabinovitz Harold S, Phelps Robert G, Cockerell Clay J, Witkowski Alexander
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.
J Clin Aesthet Dermatol. 2023 Apr;16(4):12-20.
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.
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?
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.
This was a narrative review focused on clinical use of GEP compared to other ancillary diagnostic tests performed postbiopsy.
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.
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。
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?
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。
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。
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。