Clinical guideline SEOM: hereditary colorectal cancer
Clin. transl. oncol. (Print)
; 17(12): 962-971, dic. 2015. ilus
Artigo
em Inglês
| IBECS
| ID: ibc-147434
Biblioteca responsável:
ES1.1
Localização: BNCS
ABSTRACT
Genetic mutations have been identified as the cause of inherited cancer risk in some colon cancer; these mutations are estimated to account for only 5-6 % of colorectal cancer (CRC) cases overall. Up to 25-30 % of patients have a family history of CRC that suggests a hereditary component, common exposures among family members, or a combination of both. Cancers in people with a hereditary predisposition typically occur at an earlier age than in sporadic cases. A predisposition to CRC may include a predisposition to other cancers, such as endometrial cancer. We describe genetics, current diagnosis and management of CRC hereditary syndromes pointing to a multidisciplinary approach to achieve the best results in patients and family outcomes (AU)
RESUMEN
No disponible
Texto completo:
Disponível
Coleções:
Bases de dados nacionais
/
Espanha
Base de dados:
IBECS
Assunto principal:
Placebos
/
Biópsia
/
Neoplasias Colorretais
/
Reação em Cadeia da Polimerase
/
Polipose Adenomatosa do Colo
/
Neoplasias
Tipo de estudo:
Ensaio clínico controlado
/
Guia de prática clínica
/
Estudo prognóstico
Limite:
Feminino
/
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Clin. transl. oncol. (Print)
Ano de publicação:
2015
Tipo de documento:
Artigo
Instituição/País de afiliação:
Hospital Clínico Universitario de Valencia/Spain
/
Hospital Doce de Octubre/Spain
/
Hospital General Universitario de Elche/Spain
/
Hospital La Mancha Centro/Spain
/
Hospital Marqués de Valdecilla/Spain
/
Hospital Reina Sofía/Spain
/
Hospital Universitario Ramón y Cajal/Spain
/
Hospital Universitario de Salamanca/Spain
/
Instituto Catalán de Oncología (ICO)/Spain
