| Literature DB >> 28202331 |
Panayiotis Constantinou1, Marc Tischkowitz2.
Abstract
Gynaecological cancers accounted for 16.3% of all cancers and 13.9% of all cancer deaths in women globally in 2012. Cancer of the cervix is the most common gynaecological cancer, followed by cancers of the uterus and the ovary. Although cervical cancer is almost exclusively triggered by human papilloma virus infection, approximately 5% of all uterine cancers and 20% of all ovarian cancers are caused by germline mutations in cancer predisposition genes. A number of genetic syndromes are associated with rarer gynaecological tumours. This review focuses on the epidemiology and pathology of inherited gynaecological cancer predisposition syndromes arising because of germline mutations.Entities:
Keywords: BRCA1; BRCA2; Lynch syndrome; high-throughput DNA sequencing; ovarian cancer; uterine cancer
Mesh:
Year: 2017 PMID: 28202331 DOI: 10.1016/j.bpobgyn.2017.01.004
Source DB: PubMed Journal: Best Pract Res Clin Obstet Gynaecol ISSN: 1521-6934 Impact factor: 5.237