Diagnosis of metastatic melanoma by fine-needle aspiration biopsy (FNAB) and primary melanoma using the skin and mucousa imprints

O. Grigoruk, Е. E. Pupkova, L. M. Bazulina, I. V. Vikhlyanov
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Abstract

BACKGROUND: Determination of the cytogenetic origin and morphological type of metastatic or primary tumor determines the prescription of therapy and affects to the patient’s efficiency treatment. Currently, a number of publications evaluate the potential of cytological diagnostics of melanoma.AIM: To evaluate the significance of diagnostics of metastatic melanoma by fine-needle aspiration biopsy (FNAB) and primary melanoma using the skin and mucosa imprints. MATERIALS AND METHODS In a retrospective study, a comparative analysis of cytological “melanoma” samples, in comparison with clinical and anamnestic information and the results of histological, immunohistochemical, and molecular genetic studies were carried out.Information about 109 patients from the cancer registry of the Altai Regional Oncology Dispenser (Barnaul) for 2022 was used in the work. Traditional and liquid based methods for patterns preparing were used. The samples were stained using Pappenheim and Papanicolaou methods. In some observations, cytological material was used for molecular genetic studies. Using the cancer registry data of the dispensary, the results of histological and of molecular genetic studies, and a final conclusion was given about each patient. RESULTS: Fine needle biopsy (FNA) was carried out in 80 patients. Tumor smears were obtained from 29 patients. The cytological diagnose “melanoma” was consistent with the data of histological and immunohistochemical studies (p 0.001) for all 109 patients. Melanoma was diagnosed for the first time in 64 (58.7%) patients. In other cases, the process of progression was noted from one year to 20 years. Epidermal melanoma was noted in 101 (92.7%) cases, including 9 patients with acral melanoma, and 2 cases on the vulva. Melanomas of mucosa were found in 5 cases (4.5%): in the rectum and anal canal, vagina, and in 2 cases on the hard palate. Non-epidermal (uveal) melanomas metastases were diagnosed in liver by FNAB in 3 patients (2.8%). Based on the cellular composition, epithelioid cell melanoma was determined in 91 (83.5%) patients, mixed cell in 10 (9.2%) cases, spindle cell in 6 (5.5%), pigmentless in two (1.8%) cases and nevoid melanoma(0.9%) in 1 case. The mutation status was determined in 96 patients (88.1%). Of these, in 8 patients the study was determined using cytological material. In epidermal melanomas, mutations in codon 600 of exon 15 of the BRAF gene were found in 43 (44.8%) patients, including 2 cases of acral melanoma. Mutations V600K, V600E/Ec were found in one observation (1.1; 1.1%). In mucousal melanomas: vaginal melanoma, the Q61R mutation was found in exon 3 of the NRAS gene; In anal canal melanoma, the G12C mutation was identified in exon 2 of the NRAS gene. In uveal melanomas, the assessed mutations were absent (the determining GNAQ11 and BAP1 mutations is necessary). CONCLUSIONS: Cytological diagnosis of melanoma by fine-needle aspiration biopsies and imprints from the tumor mass is a highly informative method that allows diagnosing melanoma verifying the tumor subtype.The obtained results indicate tumor heterogeneity and differences in mutational status depending on the location of melanomas. The molecular classification of melanoma is important when choosing individualized therapy.
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通过细针穿刺活检 (FNAB) 诊断转移性黑色素瘤,利用皮肤和粘膜印迹诊断原发性黑色素瘤
背景:确定转移性或原发性肿瘤的细胞遗传学来源和形态学类型决定了治疗方案的制定,并影响患者的治疗效率。目的:评估通过细针穿刺活检(FNAB)诊断转移性黑色素瘤和使用皮肤与粘膜印记诊断原发性黑色素瘤的意义。材料与方法 在一项回顾性研究中,对细胞学 "黑色素瘤 "样本进行了比较分析,并将其与临床和解剖学信息以及组织学、免疫组化和分子遗传学研究结果进行了比较。研究采用了传统的和基于液体的模式制备方法。样本采用帕本海姆法和巴氏染色法染色。在某些观察中,细胞学材料被用于分子遗传学研究。利用医务室的癌症登记数据、组织学和分子遗传学研究结果,对每位患者做出最终结论。结果:对 80 名患者进行了细针活检(FNA)。29 名患者获得了肿瘤涂片。所有 109 名患者的细胞学诊断 "黑色素瘤 "与组织学和免疫组化研究数据一致(P 0.001)。黑色素瘤在 64 例(58.7%)患者中是首次确诊。在其他病例中,黑色素瘤的发展过程从 1 年到 20 年不等。表皮黑色素瘤有 101 例(92.7%),包括 9 例尖锐湿疣黑色素瘤患者和 2 例外阴黑色素瘤患者。粘膜黑色素瘤有 5 例(4.5%),分别位于直肠和肛管、阴道,还有 2 例位于硬腭。有 3 名患者(2.8%)通过 FNAB 诊断出肝脏中的非表皮(葡萄膜)黑色素瘤转移。根据细胞组成,91 例(83.5%)患者确定为上皮样细胞黑色素瘤,10 例(9.2%)为混合细胞黑色素瘤,6 例(5.5%)为纺锤形细胞黑色素瘤,2 例(1.8%)为无色素黑色素瘤,1 例为痣样黑色素瘤(0.9%)。96名患者(88.1%)的基因突变状态得到确定。其中,8 例患者的研究是通过细胞学材料确定的。在表皮黑色素瘤中,43 例(44.8%)患者发现 BRAF 基因第 15 号外显子第 600 密码子发生突变,其中包括 2 例尖锐湿疣黑色素瘤。有 1 例患者(1.1;1.1%)发现 V600K、V600E/Ec 突变。在粘膜黑色素瘤中:阴道黑色素瘤的NRAS基因第3外显子中发现了Q61R突变;肛管黑色素瘤的NRAS基因第2外显子中发现了G12C突变。在葡萄膜黑色素瘤中,所评估的突变均不存在(需要确定 GNAQ11 和 BAP1 突变)。结论:通过细针穿刺活检和瘤块印迹对黑色素瘤进行细胞学诊断是一种信息量很大的方法,可以诊断黑色素瘤并验证肿瘤亚型。在选择个体化治疗时,黑色素瘤的分子分类非常重要。
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