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成人转移性黑色素瘤合并巨大先天性黑素细胞痣:有争议的比较基因组杂交结果

Metastatic melanoma in association with a giant congenital melanocytic nevus in an adult: controversial CGH findings.

作者信息

Machan Salma, Molina-Ruiz Ana M, Fernández-Aceñero Maria J, Encabo Beatriz, LeBoit Philip, Bastian Boris C, Requena Luis

机构信息

Departments of *Dermatology, and †Pathology, Fundación Jiménez Díaz, Universidad Autónoma, Madrid, Spain; and ‡Departments of Dermatology and Pathology, and the UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA.

出版信息

Am J Dermatopathol. 2015 Jun;37(6):487-94. doi: 10.1097/DAD.0000000000000152.

Abstract

Giant congenital melanocytic nevi (GCMNs) represent a distress to patients for 2 reasons: one is disfigurement, and the other is the increased risk of developing secondary melanocytic tumors, such as benign proliferative nodules (BPNs) and malignant melanoma (MM). BPN present as a rapid growth nodule arising within a congenital melanocytic nevus (CMN) that often ulcerates, occurs in children younger than 2 years of age. BPNs arising within a CMN are exceedingly rare after childhood, and very few cases have been described in adults. Despite the worrisome clinical and histologic findings of BPN, most laboratory investigations seem to support their benignity. The distinction between MM and BPN is extremely important, but the histopathology of BPN of GCMN can be a challenge to differentiate from MM. In the recent years, molecular tests that investigate DNA copy number alterations such as fluorescence in situ hybridization and comparative genomic hybridization have shown promise to help guide the diagnosis of ambiguous melanocytic proliferations arising within CMNs. We report the case of a 22-year-old woman with a nodule arising in a GCMN and with an axillary mass suggesting a nodal metastasis of melanoma, and discuss the unusual clinical, histopathologic, and molecular findings that make this case particularly interesting.

摘要

巨大先天性黑素细胞痣(GCMNs)给患者带来困扰有两个原因:一是毁容,二是发生继发性黑素细胞肿瘤的风险增加,如良性增生性结节(BPNs)和恶性黑色素瘤(MM)。BPN表现为先天性黑素细胞痣(CMN)内出现的快速生长结节,常发生溃疡,多见于2岁以下儿童。CMN内出现的BPN在儿童期后极为罕见,成人中仅有极少数病例报道。尽管BPN的临床和组织学表现令人担忧,但大多数实验室检查似乎支持其良性。MM与BPN的鉴别极为重要,但GCMN的BPN组织病理学与MM的鉴别可能具有挑战性。近年来,研究DNA拷贝数改变的分子检测,如荧光原位杂交和比较基因组杂交,已显示出有助于指导诊断CMN内模棱两可的黑素细胞增殖的前景。我们报告了一例22岁女性病例,其GCMN内出现结节,腋窝有肿块提示黑色素瘤淋巴结转移,并讨论了该病例不同寻常的临床、组织病理学和分子学表现,这些表现使其尤为引人关注。

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