This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages without signing in

Glucagonoma

Authoring team

This is a result of a tumour of the alpha 2 cells of the islets of Langerhans

  • the majority of these tumours are malignant
  • about 90% of patients already have liver or lymph node metastases at presentation
  • 5–20% of glucagonomas occur as component of MEN-I syndrome

This tumour may present with attacks of hyperglycaemia (diabetes mellitus occurs in more than 50% of cases), anaemia, rash and diarrhoea.

Necrolytic migratory erythema is associated with this condition (in more than 70% of patients)

  • may also affect the mucous membranes, leading to cheilitis, glossitis and stomatitis.

Other possible features include:

  • weight loss or cachexia in more than 60% of patients
  • psychiatric disturbances, such as depression or psychosis
  • tendency to venous thrombosis in about 11% of patients

Elevated fasting plasma glucagon levels are present in all patients. Also raised pancreatic polypeptide values are present in approximately 50% of patients.

Tumour localization is via techniques such as transabdominal ultrasonography, CT, MRI, selective abdominal angiography, endoscopic ultrasonography or somatostatin receptor scintigraphy.

Management:

  • directed by a specialist
  • insulin therapy may be required for diabetics
  • aspirin therapy has been used as thrombosis prophylaxis
  • octreotide is effective in controlling the rash - however this treatment modality is less effective in the management of diabetes mellitus and weight loss
    • octreotide is ineffective in reducing the incidence of venous thrombosis
  • combination chemotherapy is often given in advanced disease
  • surgical removal may be curative only for patients with local, benign disease
  • single or repeated hepatic artery embolization of the metastases initially results in symptomatic relief in the majority (more than 80%) of patients - however in more than 50% of patients the symptoms will aggravate within 6 months

Notes:

  • Zollinger-Ellison may also develop many years after the initial diagnosis (as part of MEN-I) - annual gut hormone screening has been recommended

Reference:

  1. de Herder WW and Lamberts SWJ. Best Practice & Research Clinical Endocrinology & Metabolism 2004; Volume 18(4): 477-495.

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.