Screening for Pancreatic Cancer in High-risk Populations

被引:8
|
作者
Grover, Shilpa [1 ]
Jajoo, Kunal [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Gastroenterol, 75 Francis St, Boston, MA 02115 USA
关键词
Pancreatic cancer; Hereditary; Screening; Peutz-Jeghers; BRCA; Lynch syndrome; IPMN; PanIN; PEUTZ-JEGHERS SYNDROME; FAMILY-HISTORY; GERMLINE MUTATIONS; HEREDITARY PANCREATITIS; BRCA2; MUTATIONS; INDIVIDUALS; CARCINOMA; DUCT; MANAGEMENT; NEOPLASIA;
D O I
10.1016/j.gtc.2015.10.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Pancreatic adenocarcinoma is a leading cause of cancer death. Few patients are candidates for curative resection due to the late stage at diagnosis. While most pancreatic adenocarcinomas are sporadic, approximately 10% have an underlying hereditary basis. Known genetic syndromes account for only 20% of the familial clustering of pancreatic cancer cases. The majority are due to non-syndromic aggregation of pancreatic cancer cases or familial pancreatic cancer. Screening aims to identify high-risk lesions amenable to surgical resection. However, the optimal interval for screening and the management of pancreatic cancer precursor lesions detected on imaging are controversial.
引用
收藏
页码:117 / +
页数:12
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