Hereditary colorectal cancer syndromes
Autor: | Maria Liz Leoz, Sabela Carballal, Teresa Ocaña, Leticia Moreira, Francesc Balaguer |
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Rok vydání: | 2014 |
Předmět: |
Oncology
medicine.medical_specialty Pathology medicine.diagnostic_test business.industry Colorectal cancer Gastroenterology Cancer Diagnostic evaluation medicine.disease digestive system diseases Natural history Germline mutation Internal medicine medicine Genomic information Personalized medicine business Genetic testing |
Zdroj: | Colorectal Cancer. 3:57-76 |
ISSN: | 1758-1958 1758-194X |
DOI: | 10.2217/crc.13.80 |
Popis: | SUMMARY Colorectal cancer (CRC) is one of the most common malignancies and the second-leading cause of cancer death in both sexes in developed countries. Over the last 25 years, highly penetrant monogenic germline mutations that predispose to CRC and other digestive tumors have been identified, accounting for up to 5% of all CRC cases. Identification and characterization of these disorders have allowed modification of their natural history, with a substantial decrease in morbidity and mortality among high-risk patients. Recognizing hereditary CRC has also impacted predictive genetic testing and personalized medicine based on genomic information. This review summarizes the current knowledge on hereditary CRC regarding pathogenesis, clinical features, diagnostic evaluation and management recommendations. |
Databáze: | OpenAIRE |
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