OWN RESEARCH
Using the device «Dermatoscope» manufactured by the company Scalar (Japan) facilitates the study of skin lesions with a possible magnification of up to x100 with the options of photographing and video recording and further archiving. Corresponding recommendations have been developed and indications have been determined for the application of the developed differential diagnosis algorithms in the clinical practice. All 235 patients underwent the diagnosis procedure carried out with the aid of the device «Dermatoscope» with a compulsory histologic examination of the patients subjected to surgery. The work presents basic signs typically detected in cases of nevocytic nevi, seborrheic keratosis, hemangioma, dermatofibroma.
The obtained results show that new methods of skin tumor diagnosis have been established. Such a diagnosis method should become the basic one utilized by practitioners for the detection of malignant skin tumors.
Background. Breast cancer (BC) is the most prevalent cancer in women worldwide. Genetic susceptibility to BC is heterogeneous including mutations with medium to high penetrance and single nucleotide polymorphisms (SNPs) with low penetrance. Precise assessment of genetic risk would allow to personalize the programs of prevention and treatment of BC and to reduce mortality.
Objective. We aimed to determine the frequencies of single nucleotide polymorphisms rs2981582 (FGFR2), rs3817198 (LSP1), rs889312 (5q11), rs13281615 (8q24), rs13387042 (2q35), rs3803662 (16q12) in unselected group of BC patients and healthy women in Russian population, to reveal possible associations of these polymorphisms with BC development.
Subjects and methods. An unselected group of 963 patients with BC and control group of 591 healthy female blood donors were examined. Whole peripheral blood samples were used to extract genomic DNA. Real-time polymerase chain reaction with melting curves analysis was performed for SNP genotyping.
Results: Minor allele frequencies were as follows: 41.6±1.1% and 36.2±1.1% for rs2981582 (FGFR2), 35.3±1.1% and 34.3±1.1% for rs3817198 (LSP1), 39.3±1.1% and 43.7±1.1% for rs13387042 (2q35), 27.7±1.0% and 27.8±1.0% for rs889312 (5q11), 46.2±1.1% and 44.7±1.1% for rs13281615 (8q24), 35.7±1.1% and 29.9±1.1% for rs3803662 (16q12) in group of BC patients and group of healthy women respectively. The obtained ORs for BC were 1.26 (95% CI, 1.11–1.41; p=0.003) for rs2981582, OR=0.84 (95% CI, 0.69–0.98; p=0.02) for rs13387042 and OR=1.30 (95% CI, 1.14–1.45; p=0.002) for rs3803662.
Conclusion: We confirmed the associations of previously identified SNPs rs2981582 (FGFR2), rs13387042 (2q35) and rs3803662 (16q12) with BC in Russian population.
DIAGNOSTICS AND TREATMENT OF TUMORS. ORIGINAL ARTICLES
Cancer of the cervix (cervical cancer) is one of the most common cancer and is about 12–20% of malignant neoplasms of the female genital organs [4].
Currently, cervical cancer is the second largest in the world in the incidence of all cancers of the female reproductive system, and second place in the structure of cancer mortality in women aged under 45 years, second only to breast cancer [10, 11, 12].
ISSN 2587-6813 (Online)