Synchronous and multiple renal cell carcinoma, clear cell and papillary: An approach to clinically significant genetic abnormalities

Renal Cell Cancer (RCC) is a heterogeneous disease that is characterized by distinct pathological phenotypes due to the differences in genetic alterations and signaling pathways affected (1). Bilateral renal tumors are often thought to be familial, however, they are only found in 14% of RCC cases an...

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Autores:
Cifuentes Cardona, Laura Fernanda
Martínez, Carlos Humberto
García Perdomo, Herney Andrés
Tipo de recurso:
Article of journal
Fecha de publicación:
2020
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/32803
Acceso en línea:
https://doi.org/10.1590/s1677-5538.ibju.2019.0015
https://hdl.handle.net/20.500.12494/32803
Palabra clave:
carcinoma renal
variantes genéticas
significancia clínica
renal cell carcinoma
genetic variant
clinical significance
Rights
openAccess
License
Atribución – No comercial – Sin Derivar