Pancreatic Cancer Screening of High-Risk Individuals in Arkansas

Inclusion Criteria: * Have a family history of PC as listed below or who have one of the following syndromes: Peutz-Jeghers syndrome - STK11; BRCA 1 and 2; PALB2; ATM; FAMMM / P16; HNPCC (Lynch) / MMR genes; Hereditary pancreatitis - PRSS1 * Individuals with three or more affected blood relatives (1st, 2nd or 3rd degree) * Individuals with two or more affected blood relatives with PC, with at least one affected FDR, should be considered for screening. * Patients with a history of Peutz-Jeghers syndrome should be screened, regardless of family history of PC. * Patients with a known p16 (FAMMM syndrome) with one affected 1st or 2nd degree relative will be considered for screening. * Patients with a known BRCA1 or BRCA2 mutation with one affected 1st or 2nd degree relative should be considered for screening. * Patients with a known PALB2 mutation with one affected family member should be considered for screening. * Patients with a known Mismatch-repair gene-mutation carriers (Lynch syndrome) with one affected family member should be considered for screening. Exclusion Criteria: * Not candidates for surgery