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Inherited kidney cancer syndromes
- Source :
- Current Opinion in Urology. 29:334-343
- Publication Year :
- 2019
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2019.
-
Abstract
- PURPOSE OF REVIEW To describe current paradigms for genetic testing, screening, and treatment of patients with inherited kidney cancer syndromes. RECENT FINDINGS We describe various new aspects of hereditary kidney cancer. Recent data now support that hereditary kidney cancer may account for 5-8% of kidney cancers diagnosed. Methods of testing have evolved including the introduction of multigene next-generation sequencing panels. We continue to learn more about the natural history and management of classic hereditary cancer syndromes. New emerging conditions with lower kidney cancer penetrance have been recognized adding the growing list of syndromes associated with kidney cancer development. The surgical management strategies of enucleation remain however systemic therapy options are being explored both for localized and advanced settings. SUMMARY Genetic predisposition to kidney cancer is likely more common than once thought. Knowledge of clinical manifestation and genetic testing strategies are needed to properly identify and treat patient and their families.
- Subjects :
- Urology
030232 urology & nephrology
Clinical manifestation
Bioinformatics
Systemic therapy
03 medical and health sciences
0302 clinical medicine
Neoplastic Syndromes, Hereditary
medicine
Genetic predisposition
Humans
Mass Screening
Genetic Predisposition to Disease
Genetic Testing
Carcinoma, Renal Cell
Genetic testing
Kidney
medicine.diagnostic_test
business.industry
High-Throughput Nucleotide Sequencing
medicine.disease
Penetrance
Kidney Neoplasms
Natural history
medicine.anatomical_structure
030220 oncology & carcinogenesis
business
Kidney cancer
Subjects
Details
- ISSN :
- 09630643
- Volume :
- 29
- Database :
- OpenAIRE
- Journal :
- Current Opinion in Urology
- Accession number :
- edsair.doi.dedup.....f2de5d900642ae8d6ed1d9645c0903ce
- Full Text :
- https://doi.org/10.1097/mou.0000000000000646