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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.
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页码:117 / +
页数:12
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