Hereditary Colorectal Cancer Syndromes: Familial Adenomatous Polyposis and Lynch Syndrome

详细信息    查看全文

• 作者：Wigdan Al-Sukhni ; MD^a ; ^b ; ^{wigdan.al.sukhni@utoronto.ca} ; Melyssa Aronson ; MSc ; (C) CGC^c ; Steven Gallinger ; MD ; MSc^a ; ^b
• 刊名：Surgical Clinics
• 出版年：2008
• 出版时间：August 2008
• 年：2008
• 卷：88
• 期：4
• 页码：819-844
• 全文大小：1663 K

文摘

Familial colorectal cancer (CRC) accounts for 10 % to 20 % of all cases of CRC. Two major autosomal dominant forms of heritable CRC are familial adenomatous polyposis (FAP) and Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer). Along with the risk for CRC, both syndromes are associated with elevated risk for other tumors. Improved understanding of the genetic basis of these diseases has not only facilitated the identification and screening of at-risk individuals and the development of prophylactic or early-stage intervention strategies but also provided better insight into sporadic CRC. This article reviews the clinical and genetic characteristics of FAP and Lynch syndrome, recommended screening and surveillance practices, and appropriate surgical and nonsurgical interventions.