Clinical guideline SEOM: hereditary colorectal cancer
Guillén-Ponce, C; Serrano, R; Sánchez-Heras, AB; Teulé, A; Chirivella, I; Martín, T; Martínez, E; Morales, R; Robles, L.
Clin. transl. oncol. (Print)
; 17(12): 962-971, dic. 2015. ilus
Artículo
en Inglés
| IBECS (España) | ID: ibc-147434
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)
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Asunto(s)
Humanos Masculino Femenino /normas Neoplasias Colorrectales/terapia Poliposis Adenomatosa del Colon/congénito Poliposis Adenomatosa del Colon/genética Neoplasias/metabolismo Biopsia/métodos Placebos/administración & dosificación Placebos/metabolismo Reacción en Cadena de la Polimerasa/métodos Neoplasias del Colon/tratamiento farmacológico Neoplasias Colorrectales/tratamiento farmacológico Neoplasias Colorrectales/radioterapia Poliposis Adenomatosa del Colon/metabolismo Poliposis Adenomatosa del Colon/patología Neoplasias/complicaciones Biopsia/instrumentación Placebos/provisión & distribución Reacción en Cadena de la Polimerasa
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