Nonfamilial Adenomatous Polyposis/Nonhereditary Nonpolyposis Colorectal Cancer Hereditary Polyposis and Cancer Syndromes (MAP, Syndrome-X, Muir-Torre, etc)

Autor:	Jennifer D. Rea, Daniel O. Herzig
Rok vydání:	2011
Předmět:	Oncology medicine.medical_specialty Cancer prevention business.industry Colorectal cancer Gastroenterology Cancer Disease medicine.disease Malignancy Lynch syndrome Familial adenomatous polyposis Internal medicine medicine Surgery business Syndrome x
Zdroj:	Seminars in Colon and Rectal Surgery. 22:82-87
ISSN:	1043-1489
DOI:	10.1053/j.scrs.2010.12.005
Popis:	Lynch syndrome and familial adenomatous polyposis represent the large majority of hereditary colorectal cancers; however, several additional less common syndromes are also associated with increased risk for developing malignancy. Identification of these syndromes requires an understanding of the phenotype to recognize the disease. Proper management of individuals and families affected by these syndromes provides an opportunity for cancer prevention. The purpose of this article is to provide a concise overview of the hereditary polyposis and colorectal cancer syndromes, exclusive of familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::fae8ba7db207121ce955eb65790f830a https://doi.org/10.1053/j.scrs.2010.12.005 Zobrazit plný text záznamu Full Text from ScienceDirect