Diagnosis of metastatic melanoma by fine-needle aspiration biopsy (FNAB) and primary melanoma using the skin and mucousa imprints
- Authors: Grigoruk OG1,2, Pupkova ЕE3, Bazulina LM3, Vikhlyanov IV1,2
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Affiliations:
- Altai Regional Oncology Dispensary, Barnaul, Russian Federation
- Kemerovo State Medical University», Kemerovo, Russian Federation
- Altai Regional Oncology Dispensary
- Section: Original Study Articles
- URL: https://rjonco.com/1028-9984/article/view/626586
- DOI: https://doi.org/10.17816/onco626586
- ID: 626586
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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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About the authors
O G Grigoruk
Altai Regional Oncology Dispensary, Barnaul, Russian Federation;Kemerovo State Medical University», Kemerovo, Russian Federation
Author for correspondence.
Email: cytolakod@rambler.ru
ORCID iD: 0000-0001-9981-2348
MD, Head of the Cytology Laboratory «Altai Regional Oncology Dispanser», 656045, Zmeinogorskiy tract, 110 к,
Professor «The Kemerovo State Medical University», Kemerovo, Russian Federation
Russian Federation, 656045, Алтайский край, г Барнаул, Змеиногорский тракт, 110к; 650056, г Кемерово,. ул. Ворошилова 22аЕ E Pupkova
Altai Regional Oncology Dispensary
Email: elenapupkova@yandex.ru
ORCID iD: 0000-0001-7369-1883
MD, Head of the Laboratory «Altai Regional Oncology Dispanser»
Russian Federation, 656045, Алтайский край, г Барнаул, Змеиногорский тракт, 110к
L M Bazulina
Altai Regional Oncology Dispensary
Email: lardoc69@mail.ru
ORCID iD: 0000-0002-7222-0657
Dr. of the Cytology Laboratory "Altai Regional Oncology Dispanser"
Russian Federation, 656045, Алтайский край, г Барнаул, Змеиногорский тракт, 110кI V Vikhlyanov
Altai Regional Oncology Dispensary, Barnaul, Russian Federation;Kemerovo State Medical University», Kemerovo, Russian Federation
Email: akod@akod22.ru
ORCID iD: 0000-0003-3290-7187
MD,Chief Medical Officer «Altai Regional Oncology Dispanser»,
Professor «The Kemerovo State Medical University», Kemerovo, Russian Federation
Russian Federation, 656045, Алтайский край, г Барнаул, Змеиногорский тракт, 110к; 650056, г Кемерово,. ул. Ворошилова 22аReferences
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