Glucagonoma (patient information)
For the WikiDoc page for this topic, click here
Editor-in-Chief: Jinhui Wu, MD
Please Join in Editing This Page and Apply to be an Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
What is glucagonoma?
Glucagonoma is a very rare tumor of the islet cells of the pancreas which is an organ in the abdomen that can make insulin and glucagon to regulate blood sugar level. A patient of insulinoma can produce too much glucagon. Patients may show a series of symptoms of hyperglucagonemia and hypoaminoacidemia, such as anemia, diarrhea, weight loss, necrolytic migratory erythema and Diabetes Mellitus. Treatments invlove surgery and medication.
How do I know if I have glucagonoma and what are the symptoms of glucagonoma?
Usual symptoms of glucagonoma invlove a series of signs of hyperglucagonemia and hypoaminoacidemia:
- Excess thirst
- Increased appetite
- Inflamed mouth and tongue
- Skin rash
Other health problems may also cause these symptoms. Only a doctor can tell for sure. A person with any of these symptoms should tell the doctor so that the problems can be diagnosed and treated as early as possible.
Who is at risk for glucagonoma?
The cause of insulinoma is not clear.
How to know you have glucagonoma?
- Blood test: The patient needs to test fasting glucose level and serum glucagon level. In patients with glucagonoma, the level of the two are great higer than normal.
- Oral glucose tolerance test: This is one of the tools used to diagnose Diabetes Mellitus.
- Complete blood count: A patient with glucagonoma may show anemia.
- Skin biopsy: Skin biopsy is a good test for skin lesions. Pathologists may find necrolytic migratory erythema in patients with glucagonoma.
- Computed tomography (CT) scan: CT scans are often used to diagnose glucagonoma. It can confirm the location of the tumor and show the organs nearby. These are helpful for determining the stage of the cancer and in determining whether surgery is a good treatment option.
- Magnetic resonance imaging (MRI): An MRI uses magnetic fields but it is a different type of image than what is produced by computed tomography (CT) and produces detailed images of the body. Like computed tomography (CT), a contrast agent may be injected into a patient’s vein to create a better picture.
- Positron emission tomography (PET) scan: When doing this test, a small amount of a radioactive medium is injected into your body and absorbed by the organs or tissues. This radioactive substance gives off energy which in turn is used to produce the images. PET can provide more helpful information than either CT or MRI scans. It is useful to see if the cancer has spread to the lymph nodes and it is also useful for your doctor to locate where the cancer has spread.
When to seek urgent medical care?
Call your health care provider if symptoms of glucagonoma develop. If you experience either of the following symptoms, seeking urgent medical care as soon as possible:
- Severe diarrhea
Treatment options
For patients with glucagonoma, surgery is the definitive management. Before treatment starts, ask your health care team about possible side effects and how treatment may change your normal activities.
- Surgery: The surgical measure may involve surgical removal of the glucagonoma. It is the first preferred treatment for the patients.
- Medication: For patients who may not accept surgery, medications such as octreotide, doxorubicin and streptozotocin can be used to block the release of glycagon.
Diseases with similar symptoms
SKin lesions
Where to find medical care for glucagonoma?
Directions to Hospitals Treating glucagonoma