Other Names for this Disease
- Vasoactive intestinal peptide (VIP) tumor
- Pancreatic VIPoma
- Vasoactive intestinal peptide-producing tumor
- Diarrheogenic islet cell tumor
- VIP-secreting tumor
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dehydration, and low blood potassium (hypokalemia). VIPomas are usually diagnosed in adults around age 50. The cause of VIPoma is unknown. Treatment may include intravenous (IV) fluids to correct dehydration, medications such as octreotide to help control diarrhea, and surgery to remove the tumor.VIPoma is a rare cancer that develops within the pancreas. This tumor causes pancreatic cells to produce high levels of a hormone called vasoactive intestinal peptide (VIP). The signs and symptoms of a VIPoma include abdominal pain, flushing or redness of the face, nausea, watery diarrhea, weight loss,
Last updated: 3/8/2010
- Stitham SO. VIPoma. MedlinePlus Web site. September 4, 2008; http://www.nlm.nih.gov/medlineplus/ency/article/000228.htm. Accessed 3/8/2010.
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- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss VIPoma. Click on the link to view a sample search on this topic.