| Literature DB >> 26979427 |
A Agaimy1, A Hartmann2.
Abstract
Renal cell carcinomas are associated with hereditary tumor syndromes in approximately 5 % of cases. In patients with a hereditary predisposition, tumors show an earlier age of onset, often with a multicentric and bilateral manifestation. While some patients with renal cell carcinoma can be classified into well-characterized kidney cancer syndromes others have a genetic background which is still poorly understood. Most of the specific tumor syndromes are associated with a histopathologically distinct renal cell tumor phenotype. The recognition of patients with hereditary renal cell carcinoma and the identification of individual family members with a higher risk of development of renal tumors is important for early tumor detection and treatment. This manuscript reviews the clinical pathological and molecular findings of hereditary renal cell carcinoma syndromes.Entities:
Keywords: Early tumor recognition; Genetic predisposition; Human genetic clarification; Renal cell carcinoma; Von Hippel-Lindau syndrome
Mesh:
Year: 2016 PMID: 26979427 DOI: 10.1007/s00292-016-0153-0
Source DB: PubMed Journal: Pathologe ISSN: 0172-8113 Impact factor: 1.011