TTD consensus document on the diagnosis and management of hereditary colorectal cancer


Por: Segura, PP, Alonso, CG, Cajal, TRY, Blanch, RS, Aranda, E

Publicada: 1 may 2010
Resumen:
Colorectal cancer is the first cause of cancer in occidental countries if we consider both male and females tumours. In Spain, 26,000 new cases are diagnosed every year. The possibilities of cure are higher if the tumour is diagnosed early. One of the most important risk factors for colorectal cancer is inheritance. Some hereditary syndromes, such as familial adenomatous polyposis (FAP), increase the risk by almost 100% and at a young age. Other more prevalent syndromes, such Lynch syndrome, increase the risk 10-12 times more than in the general population. This article aims at summarising the most important aspects in hereditary colorectal cancer and to be a useful tool to oncologists who work with these patients and their families.

Filiaciones:
Segura, PP:
 Hosp Clin San Carlos, Dept Med Oncol, ES-28040 Madrid, Spain

Alonso, CG:
 Hosp Ramon & Cajal, Dept Med Oncol, Madrid, Spain

Cajal, TRY:
 Hosp Santa Creu & Sant Pau, Dept Med Oncol, Barcelona, Spain

Blanch, RS:
 Hosp Reina Sofia, Dept Med Oncol, Cordoba, Spain

Aranda, E:
 Hosp Reina Sofia, Dept Med Oncol, Cordoba, Spain
ISSN: 1699048X





Clinical & Translational Oncology
Editorial
SPRINGER INTERNATIONAL PUBLISHING AG, GEWERBESTRASSE 11, CHAM, CH-6330, SWITZERLAND, España
Tipo de documento: Article
Volumen: 12 Número: 5
Páginas: 356-366
WOS Id: 000208266400007
ID de PubMed: 20466620

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