This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

Muir-Torre Syndrome

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

The Muir-Torre Syndrome describes a rare assembly of conditions:

  • sebaceous tumours
  • internal malignancies
  • keratoacanthomas - are not mandatory to the diagnosis

It is an autosomal dominant condition that has been linked to chromosome 2p. The sebaceous tumours are usually multiple and ranging in type from adenomata to carcinomata. These can co-exist with multiple and occasionally very large keratoacanthoma.

Internal malignancies associated with the condition are:

  • colonic cancer and polyposis coli
  • carcinoma of larynx
  • carcinoma of endometrium

Long-term retinoic acid has been used to treat 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.