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 Ninty percent of insulinomas are benign (noncancerous). In most cases, the underlying cause of insulinoma is unknown. However, people with specific genetic syndromes such as multiple endocrine neoplasia type I, Von Hippel-Lindau syndrome, Neurofibromatosis type 1, and tuberous sclerosis are at risk of insulinomas and other endocrine tumors. Treatment generally includes surgery to remove the tumor.Insulinoma is a type of pancreatic neuroendocrine tumor (pancreatic NET), which refers to a group of rare tumors that form in the hormone-making cells of the pancreas. Insulinomas, specifically, produce too much insulin, a hormone that reduces the level of sugar in the blood by helping it move into cells. As a result, people with insulinomas generally have very low blood sugar levels which can be associated with anxiety, confusion, hunger, a fast heart rate, and sweating. In severe cases, it can lead to seizures, coma or even death.
Last updated: 4/26/2016
- Insulinoma. MedlinePlus. October 2014; https://www.nlm.nih.gov/medlineplus/ency/article/000387.htm.
- Zonera Ashraf Ali, MBBS. Insulinoma. Medscape Reference. February 2016; http://emedicine.medscape.com/article/283039-overview.
- F John Service, MD, PhD. Insulinoma. UpToDate. November 2015;
- Pancreatic Neuroendocrine Neoplasms. NORD. 2014; http://rarediseases.org/rare-diseases/pancreatic-neuroendocrine-neoplasms-pnens/.
- Johns Hopkins Medicine offers an information page on Insulinoma Please click on the link to access this resource.
- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic.
- The National Cancer Institute provides the most current information on cancer for patients, health professionals, and the general public.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.