Hereditary Renal Cell Carcinoma Syndromes.

BAP1-Tumor predisposition syndrome Birt–Hogg–Dubé Fumarate hydratase Genetic risk Genetic testing Hereditary leiomyomatosis and renal cell carcinoma Hereditary renal cell carcinoma Von hippel-lindau

Journal

Hematology/oncology clinics of North America
ISSN: 1558-1977
Titre abrégé: Hematol Oncol Clin North Am
Pays: United States
ID NLM: 8709473

Informations de publication

Date de publication:
10 2023
Historique:
medline: 18 9 2023
pubmed: 1 6 2023
entrez: 31 5 2023
Statut: ppublish

Résumé

Up to 5% of renal cell carcinomas (RCCs) can be associated with a known hereditary RCC syndrome. In addition to the well-characterized RCC syndromes, there are also emerging syndromes associated with increased RCC risk. In the last few years, consensus guidelines have outlined recommendations for who should be referred for genetic evaluation, and what screening should be done for early detection of RCC. Although much progress has been made, work is still needed-guidelines are still mostly based on expert opinion and the role of emerging genetic associations will need to be clarified.

Identifiants

pubmed: 37258351
pii: S0889-8588(23)00047-3
doi: 10.1016/j.hoc.2023.04.013
pii:
doi:

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

841-848

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Maria I Carlo (MI)

Genitourinary Oncology Service, Clinical Genetics Service, Memorial Sloan Kettering Cancer Center, 353 East 68th Street. New York, NY 10065, USA. Electronic address: carlom@mskcc.org.

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Classifications MeSH