| Literature DB >> 28567709 |
Georgios Kallinikas1, Helai Habib2, Dimitrios Tsimiliotis3, Evangelos Koutsokostas4, Barna Bokor5.
Abstract
The prevalence of RCC in Europe is 2-3% and increasing every year. Hereditary predisposition is found in 5-8% of all RCC cases. Hereditary syndromes associated with RCC include: Von Hippel-Lindau, hereditary papillary renal cell carcinoma, Birt-Hogg-Dube', hereditary leiomyomatosis, succinate dehydrogenase's deficiency, tuberous sclerosis complex and Cowden's syndrome. These syndromes are related to specific genetic mutations. So far the European Association of Urology and American Urological Association have not established guidelines for referral of patients with RCC for germline mutation screening. The scope of this article is to review which clinical manifestations should direct clinicians' thinking towards hereditary kidney carcinomas and therefore suggest which patients could benefit from genetic testing.Entities:
Keywords: Genetic counseling; Genetic testing; Germline mutation; Kidney neoplasms; Renal cell carcinoma; Von Hippel–Lindau
Mesh:
Substances:
Year: 2017 PMID: 28567709 DOI: 10.1007/s11255-017-1625-8
Source DB: PubMed Journal: Int Urol Nephrol ISSN: 0301-1623 Impact factor: 2.370