Fatal Spitz Melanoma With MAD1L1::BRAF Fusion: A Case Report and Literature Review.

IF 1.6 4区 医学 Q3 DERMATOLOGY
Tsubasa Hiraki, Satoshi Hirakawa, Yoshiro Otsuki, Kazuyoshi Kajimoto, Keisuke Goto, Masakuni Serizawa
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Abstract

Spitz melanoma is extremely rare, and only a few cases of distant metastases have been reported. Herein, we describe a case of Spitz melanoma with multiple distant metastases. A 37-year-old woman presented with a 5.5-mm-diameter nodule on the right lower leg. She experienced multiple distant metastases, involving the lungs, liver, thyroid, stomach, ovary, bones, and skin, along with multiple lymph node metastases within 1 year. The patient succumbed to the disease 1 year and 6 months following the first excision. Histopathological examination revealed a dense distribution of large solid nests comprising large, atypical epithelioid melanocytes with abundant eosinophilic cytoplasm in the upper dermis. Diffuse PRAME and loss of p16 immunoexpression profiles were observed. Targeted DNA and Sanger sequencing revealed an in-frame MAD1L1(e16)::BRAF(e9) fusion in both primary tumor and metastatic subcutaneous lesion. A review of previously reported cases confirmed as Spitz melanoma with distant metastases (n = 7) revealed a broad age range (11-71 years, median 46 years), high mortality (5/7), frequent BRAF fusions (6/7), and recurrent TERT promotor mutations and CDKN2A/B deletions. This report adds valuable insights into our understanding of the clinical and genetic characteristics of Spitz melanoma with distant metastases.

伴有MAD1L1::BRAF融合的致死性Spitz黑色素瘤1例报告及文献回顾
Spitz黑色素瘤极为罕见,只有少数远处转移的病例被报道过。在此,我们描述了一例多发性远处转移的Spitz黑色素瘤。37岁女性,右小腿有直径5.5 mm的结节。她经历了多次远处转移,累及肺、肝、甲状腺、胃、卵巢、骨骼和皮肤,并在1年内发生了多次淋巴结转移。患者在第一次手术后1年零6个月死亡。组织病理学检查显示真皮上部致密分布的大实心巢,包括大的非典型上皮样黑色素细胞和丰富的嗜酸性细胞质。观察到弥漫性PRAME和p16免疫表达谱的缺失。靶向DNA和Sanger测序显示,原发性肿瘤和转移性皮下病变中均存在框架内MAD1L1(e16)::BRAF(e9)融合。对先前报道的Spitz黑色素瘤远处转移病例(n = 7)的回顾显示,年龄范围广(11-71岁,中位46岁),死亡率高(5/7),BRAF融合频繁(6/7),复发TERT启动子突变和CDKN2A/B缺失。本报告为我们对Spitz黑色素瘤远处转移的临床和遗传特征的理解增加了有价值的见解。
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
CiteScore
3.20
自引率
5.90%
发文量
174
审稿时长
3-8 weeks
期刊介绍: Journal of Cutaneous Pathology publishes manuscripts broadly relevant to diseases of the skin and mucosae, with the aims of advancing scientific knowledge regarding dermatopathology and enhancing the communication between clinical practitioners and research scientists. Original scientific manuscripts on diagnostic and experimental cutaneous pathology are especially desirable. Timely, pertinent review articles also will be given high priority. Manuscripts based on light, fluorescence, and electron microscopy, histochemistry, immunology, molecular biology, and genetics, as well as allied sciences, are all welcome, provided their principal focus is on cutaneous pathology. Publication time will be kept as short as possible, ensuring that articles will be quickly available to all interested in this speciality.
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