Undifferentiated melanoma: a molecular study of a fatal metastatic "atypical fibroxanthoma (AFX)".

IF 3.1 3区 医学 Q1 PATHOLOGY
Simon Haefliger, Baptiste Ameline, Veronika Blum, Matthias S Matter, Beata Bode-Lesniewska
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引用次数: 0

Abstract

Diagnosing undifferentiated spindle cell and pleomorphic tumours of the sun-exposed skin of elderly patients is common and challenging. This paper presents the case of a 64-year-old man with a tumour that was initially diagnosed as an atypical fibroxanthoma, but which metastasised to the bone and lung, resulting in death within two years. Extensive comparative molecular studies were performed using next-generation sequencing (NGS) and methylomic analysis, which demonstrated that the skin tumour and the bone metastases corresponded to the same neoplasms. In addition to other aberrations, NGS analysis of both tumour manifestations revealed NF1 gene mutations, suggesting a diagnosis of undifferentiated melanoma. Interestingly, however, the methylomic analysis grouped the tumours with the "atypical fibroxanthoma/pleomorphic dermal sarcoma (AFX/PDS)" class of the reference cases, rather than with conventional or desmoplastic melanomas. Molecular studies may help to reveal the genetic basis of difficult-to-classify undifferentiated skin neoplasms as well as help to estimate their biological potential.

未分化黑色素瘤:致命转移性“非典型纤维黄色瘤(AFX)”的分子研究。
诊断未分化梭形细胞和多形性肿瘤的老年患者暴露在阳光下的皮肤是常见和具有挑战性的。本文介绍了一名64岁男子的肿瘤,最初被诊断为非典型纤维黄色瘤,但转移到骨骼和肺部,导致两年内死亡。使用下一代测序(NGS)和甲基组学分析进行了广泛的比较分子研究,证明皮肤肿瘤和骨转移对应于相同的肿瘤。除了其他畸变外,两种肿瘤表现的NGS分析显示NF1基因突变,提示未分化黑色素瘤的诊断。然而,有趣的是,甲基组学分析将肿瘤归为“非典型纤维黄色瘤/多形性真皮肉瘤(AFX/PDS)”一类的参考病例,而不是传统的或纤维增生性黑色素瘤。分子研究可能有助于揭示难以分类的未分化皮肤肿瘤的遗传基础,并有助于估计其生物学潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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