This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Pathology

Authoring team

The fundamental defect is a failure of hepatic excretion of copper into bile - copper accumulates in the liver and secondarily suppresses the synthesis of caeruloplasmin. Eventually, copper spills over into the circulation and deposits also in the:

  • basal ganglia - with neurological sequalae
  • kidneys - causing tubuar degeneration and thus a Fanconi syndrome
  • cornea - with Kayser-Fleischer rings
  • bones and joints, with erosions
  • parathyroid glands

Histological appearances of the liver are not diagnostic and vary from that of chronic active hepatitis to a macronodular cirrhosis. Copper staining may reveal a periportal distribution.


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.