| Literature DB >> 21633635 |
Alina Stoita1, Ian D Penman, David B Williams.
Abstract
Pancreatic cancer is difficult to diagnose at an early stage and is associated with a very poor survival. Ten percent of pancreatic cancers result from genetic susceptibility and/or familial aggregation. Individuals from families with multiple affected first-degree relatives and those with a known cancer-causing genetic mutation have been shown to be at much higher risk of developing pancreatic cancer. Recent efforts have focused on detecting disease at an earlier stage to improve survival in these high-risk groups. This article reviews high-risk groups, screening methods, and current screening programs and their results.Entities:
Keywords: Cancer screening; Endoscopic ultrasound; Familial cancer; Hereditary cancer; Pancreatic cancer; Risk factors
Mesh:
Year: 2011 PMID: 21633635 PMCID: PMC3103788 DOI: 10.3748/wjg.v17.i19.2365
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742