This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Osler - Weber - Rendu syndrome

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Hereditary haemorrhagic telangiectasia is a rare autosomal dominant condition where multiple small telangiectases occur on the skin and mucous membranes, most commonly on the lips and the tongue. Lesions are also often scattered over the pulps of fingers. The size and number of lesions increases with age.

Epistaxis is the most common complaint.

When telangiectases are present in the gastrointestinal tract they may cause chronic blood loss with iron deficiency anaemia. Occasionally there may be torrential bleeding.

Arteriovenous malformations may occur in the:

  • liver
  • lungs, causing:
    • clubbing
    • murmurs
    • paradoxical emboli

Oestrogen may be used to reduce the severity and frequency of epistaxes (via induction of metaplasia of nasal mucosa).

Embolization may be used if there are pulmonary arteriovenous malformations.

Click here for an image of this condition

 


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.