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伴有LMNA::NTRK1融合的巨大先天性黑素细胞痣:为先天性痣和黑色素瘤拓展靶向治疗选择

Large Congenital Melanocytic Nevus With LMNA::NTRK1 Fusion: Expanding Targeted Therapy Options for Congenital Nevi and Melanoma.

作者信息

Nagarkar Akanksha, Turbeville Jackson, Hinshaw Molly A, LeBoit Philip E, Gagan Jeffrey, Raffeld Mark, Aldape Kenneth, Shah Niharika, Barr Frederic G, Xi Liqiang, Lee Ina, Ferrone Christina K, Pack Svetlana D, Kaplan Rosandra, Malone Mary Frances Wedekind, Yohe Marielle, Sargen Michael R

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, United States.

Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, United States.

出版信息

J Cutan Pathol. 2025 Aug;52(8):523-527. doi: 10.1111/cup.14822. Epub 2025 Jun 3.

Abstract

Large congenital melanocytic nevi/nevus (LCMN) are caused by genetic events that activate the mitogen-activated protein kinase (MAPK) and extracellular signal-regulated kinase (ERK) pathway. Individuals with LCMN are prone to developing aggressive melanomas during childhood. Targeted therapies are needed to treat this form of melanoma and manage LCMN symptoms such as pruritus and pain, which significantly impact quality of life. Here, we present the first case of an LCMN with an NTRK fusion driver event. The patient presented with an atypical proliferative nodule arising in the background nevus. RNA sequencing of the proliferative nodule with background nevus identified a pathogenic LMNA::NTRK1 fusion. The fusion resulted in constitutive expression of TrkA, demonstrated by strong cytoplasmic pan-TRK staining, along with activation of the MAPK/ERK pathway, as indicated by positive nuclear and cytoplasmic staining for phosphorylated ERK. The background nevus beneath the proliferative nodule also expressed pan-TRK and phosphorylated ERK, suggesting that the NTRK1 fusion occurred prior to the formation of the proliferative nodule. This case broadens the spectrum of driver events for LCMN and suggests that screening for TRK fusions in LCMN should be considered when systemic therapy is being considered for melanoma or symptom management.

摘要

巨大先天性黑素细胞痣(LCMN)由激活丝裂原活化蛋白激酶(MAPK)和细胞外信号调节激酶(ERK)通路的遗传事件引起。患有LCMN的个体在儿童期易患侵袭性黑色素瘤。需要有针对性的治疗来治疗这种形式的黑色素瘤并控制LCMN症状,如瘙痒和疼痛,这些症状会显著影响生活质量。在此,我们报告首例伴有NTRK融合驱动事件的LCMN病例。患者表现为在背景痣中出现的非典型增生性结节。对增生性结节及背景痣进行RNA测序,发现了致病性的LMNA::NTRK1融合。这种融合导致TrkA的组成性表达,表现为强烈的细胞质泛TRK染色,同时MAPK/ERK通路激活,表现为磷酸化ERK的细胞核和细胞质染色阳性。增生性结节下方的背景痣也表达泛TRK和磷酸化ERK,提示NTRK1融合发生在增生性结节形成之前。该病例拓宽了LCMN驱动事件的范围,并表明在考虑对黑色素瘤进行全身治疗或症状管理时,应考虑对LCMN进行TRK融合筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ef6/12232092/07fd5efa374b/CUP-52-523-g002.jpg

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