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MEN I - glucagonoma DefinitionGlucagonoma is a very rare tumor of the islet cells of the pancreas, which leads to an excess of the hormone glucagon in the blood. CausesGlucagonoma is usually cancerous (malignant). The cancer tends to spread and get worse if not treated. This cancer affects some of the islet cells of the pancreas. As a result, the affected islet cells produce too much of the hormone glucagon. The cause is unknown. Genetic factors play a role in some cases. A family history of the syndrome multiple endocrine neoplasia type I (MEN I) is a risk factor. SymptomsSymptoms of glucagonoma may include any of the following:
In most cases, the cancer has already spread to the liver when it is diagnosed. Exams and TestsThe health care provider will perform a physical exam and ask about your medical history and symptoms. Tests that may be done include: TreatmentSurgery to remove the tumor before it spreads is usually recommended. Chemotherapy may be done when surgery is not possible. Support GroupsYou can ease the stress of illness by joining a cancer support group. Sharing with others who have common experiences and problems can help you not feel alone. Outlook (Prognosis)Approximately 60% of these tumors are cancerous. It is common for this cancer to spread to the liver. Only about 20% of people can be cured with surgery. If the tumor is only in the pancreas and surgery to remove it is successful, people have a 5-year survival rate of 85%. Possible ComplicationsThe cancer can spread to the liver. High blood sugar level can cause problems with metabolism and tissue damage. When to Contact a Medical ProfessionalContact your provider if you notice symptoms of glucagonoma. ReferencesAsban A, Patel AJ, Reddy S, Wang T, Balentine CJ, Chen H. Cancer of the endocrine system. In: Niederhuber JE, Armitage JO, Kastan MB, Doroshow JH, Tepper JE, eds. Abeloff's Clinical Oncology. 6th ed. Philadelphia, PA: Elsevier; 2020:chap 68. National Cancer Institute website. Pancreatic neuroendocrine tumors (islet cell tumors) treatment (PDQ) - health professional version. www.cancer.gov/types/pancreatic/hp/pnet-treatment-pdq. Updated August 19, 2022. Accessed December 15, 2022. Newey PJ, Thakker RV. Multiple endocrine neoplasia. In: Melmed S, Auchus RJ, Goldfine AB, Koenig RJ, Rosen CJ, eds. Williams Textbook of Endocrinology. 14th ed. Philadelphia, PA: Elsevier; 2020:chap 42. | |
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Review Date: 10/16/2022 Reviewed By: Mark Levin, MD, Hematologist and Oncologist, Monsey, NY. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team. The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. No warranty of any kind, either expressed or implied, is made as to the accuracy, reliability, timeliness, or correctness of any translations made by a third-party service of the information provided herein into any other language. © 1997- A.D.A.M., a business unit of Ebix, Inc. Any duplication or distribution of the information contained herein is strictly prohibited. | |