This site is intended for healthcare professionals

Sign in
Go to /sign-in page

You can view 5 more pages before signing in

Peutz-Jegher's syndrome

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Peutz-Jegher's syndrome is an autosomal dominant condition characterised by:

  • multiple hamartogenous polyps of the gastrointestinal tract - most often in the small bowel but may occur affect any portion of the GI tract
  • mucocutaneous pigmentation - mainly, of the lips, buccal mucosa, genitalia, hands and feet

Patients often present with small bowel intussusception before the age of 10 years.

The polyps themselves have a very low malignant potential. About 10-20% of patients develop gastrointestinal carcinoma but this is thought to arise from coexistent adenomas.

Patients have an increased risk of developing carcinomas of the pancreas, lung, ovary and breast.

Click here for an example image of this condition

 

Related pages

Create an account to add page annotations

Create a free account

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed 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.