Pancreatic Cancer
Approximately 1 in 76 people will develop pancreatic cancer in their lifetime. Most pancreatic cancer develops by chance and does not run in families. However, some pancreatic cancers are hereditary. Hereditary cancers are caused by a mutation in a gene that can be passed on from generation to generation.
Symptoms
- Yellow skin and eyes, darkening of the urine, itching, and clay-colored stool
- Pain in the upper abdomen or upper back
- Loss of appetite, nausea, or vomiting
- Unexplained weight loss
Causes/Risk Factors
- Smoking
- Obesity or high fat diet
- Diabetes
- History of chronic pancreatitis (inflammation of the pancreas)
- Family history of pancreatic cancer, breast cancer, or melanoma
- Genetic mutations
Genetic Test
The following genetic tests may be appropriate based on your personal and/or family history:
- BRCA1/2 (hereditary breast and ovarian cancer syndrome)
- MLH1, MSH2, MSH6, PMS2 (Lynch syndrome/HNPCC)
- p16 (hereditary melanoma)
- PRSS1, CFTR, SPINK1 (hereditary pancreatitis)
- STK11 (Peutz-Jeghers syndrome)
- Genetic variants for pancreatic cancer
Schedule an Appointment
To speak with a board-certified genetic counselor about your risks for this disease:
Learn more about scheduling.
Learn More
American Cancer Society
Support Groups
The National Pancreas Foundation
Pancreatic Cancer Action Network (PanCAN)
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