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Glucagonoma
* Glucagonoma: Neuroendocrine Tumor of pancreatic islet cells that leads to elevated levels of
glucagon
.
Rare
Usually solitary, sporadic, and present in patients 50+ y.o.
Inherited forms are associated with
MEN 1
Pathophysiology:
Glucagon acts on the liver to increase gluconeogenesis and amino acid oxidation.
Patients often experience weight loss, diarrhea, necrolytic migratory erythema, venous thrombosus, and glucose intolerance (
diabetes mellitus
). Many experience neuropsychiatric abnormalities.
Diagnosis: Symptoms, elevated glucagon, and imaging studies.
Treatment: treat diabetes, nutritional supplementation, and Somatostatin analogs to counter glucagon hypersection.
Often metastatic, particularly to the liver and bones, via the lymph nodes.
Related Tutorials
Multiple Endocrine Neoplasia (MEN)
Insulin, Glucagon, & Glucose Homeostasis
Glucagon Secretion & Physiology