Malignant neoplasms, including pancreatic cancer and melanoma, are major global health challenges. This study investigates melanoma pancreatic syndrome, a rare hereditary tumor syndrome associated with gene mutations. mutations contribute to a lifetime risk of melanoma ranging from 28% to 67%.
View Article and Find Full Text PDFObjective: Describe the structure of pathogenic germline variants and clinical and anatomical features in colorectal cancer patients in Moscow.
Material And Methods: The whole genome sequencing results of patients with suspected hereditary cancer syndrome were evaluated. All identified genetic variants were validated using Sanger sequencing.
More than 275 million people in the world are carriers of a heterozygous mutation of the gene, associated with cystic fibrosis, the most common autosomal recessive disease among Caucasians. Some recent studies assessed the association between carriers of variants and some pathologies, including cancer risk. The aim of this study is to analyze the landscape of germline pathogenic heterozygous variants in patients with diagnosed malignant neoplasms.
View Article and Find Full Text PDFThere is more than 58-year experience of surgical treatment of patients with intracardiac myxomas at the Petrovsky National Research Center of Surgery. Primary delayed growth of the right and left atrial myxoma after 21 years and 5 months was observed only in 1 (0.36%) patient.
View Article and Find Full Text PDFGeorgian Med News
June 2019
Unlabelled: Objective - to conduct a systematic analysis of the data available in the modern literature on non-rectoscopic endometrial ablation (NRAE).
Materials And Methods: The review includes data from world studies for the last 7 years.
Results: second generation systems based on different surgical energies and parameters of their performance.