At a Glance
Glucagonoma (“sweet” syndrome) is one of the functioning pancreatic neuroendocrine tumors (NETs) that account for 1-3% of all pancreatic NETs. Most cases are sporadic, but 5-17% are associated with multiple endocrine neoplasia type 1 (MEN1). Glucagonomas are typically single, large tumors (average size 6 cm) and are found almost exclusively in the pancreas. The tumors are malignant in 80-90% of cases; however, as for other NETs, the degree of malignancy cannot be predicted by histological appearance. Glucagonomas present with liver metastases in more than 60% of cases
Glucagonomas present clinically with glucose intolerance (40-90%) or diabetes (with associated marked weight loss in 80% of cases), accompanied by the “4D syndrome,” including dermatosis (necrolytic migratory erythema in 70-90% of cases), depression, deep venous thrombosis (30% of cases), and diarrhea. Glucose intolerance in the glucagonoma syndrome may relate to tumor size. Many symptoms are nonspecific, but the presence of necrolytic migratory erythema should prompt evaluation of glucagonoma.
What Tests Should I Request to Confirm My Clinical Dx? In addition, what follow-up tests might be useful?
Diagnosis of a glucagonoma requires demonstration of increased plasma glucagon concentrations (usually 500-1000 pg/mL, reference interval <50 pg/mL) in the presence of clinical symptoms. Concentrations are markedly higher than those reported in healthy, fasting subjects (<150 pg/ mL) or in other disorders causing hyperglucagonemia, including diabetes mellitus, burn injury, acute trauma, bacteremia, acute pancreatitis, cirrhosis, Cushing syndrome, and renal and hepatic failure (<500 pg/mL). However, some glucagonoma patients have glucagon concentrations in the “physiologically elevated” range. Therefore, in patients with a classic clinical presentation, a serum glucagon concentration less than 500 pg/mL does not exclude a glucagonoma. Concentrations greater than 1000 pg/mL are virtually diagnostic of the disease.
Serum chromogranin A (CGA) is a nonspecific marker for well-differentiated neuroendocrine tumors that does not distinguish the various tumor subtypes. CGA is usually increased in gastroenteropancreatic neuroendocrine tumors (GEP-NETs), including glucagonomas. CGA concentration correlates with tumor volume and may be useful for staging, prognosis, and monitoring. CGA is elevated in other conditions, including renal insufficiency and severe malabsorption syndrome.
After the diagnosis is made, the glucagonoma must be located and staged with the use of imaging studies (for patients who are surgical candidates).(Table 1)
Are There Any Factors That Might Affect the Lab Results? In particular, does your patient take any medications – OTC drugs or Herbals – that might affect the lab results?
CGA results may be elevated in patients with renal insufficiency or severe malabsorption syndrome.
What Lab Results Are Absolutely Confirmatory?
Histopathological evaluation (with the use of ancillary studies, including immunohistochemical stains for neuroendocrien markers if necessary) of the removed tumor or biopsy material confirms the diagnosis.
Additional Issues of Clinical Importance
Delayed diagnosis can lead to adverse effects, including long-term risks associated with diabetes mellitus, as well as postponed treatment of the underlying condition, which is primarily surgical.
Errors in Interpretation of Test Results
In patients with a classic clinical presentation, a serum glucagon concentration less than 500 pg/mL does not exclude a glucagonoma.
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- At a Glance
- What Tests Should I Request to Confirm My Clinical Dx? In addition, what follow-up tests might be useful?
- Are There Any Factors That Might Affect the Lab Results? In particular, does your patient take any medications - OTC drugs or Herbals - that might affect the lab results?
- What Lab Results Are Absolutely Confirmatory?
- Additional Issues of Clinical Importance
- Errors in Interpretation of Test Results