Pigmented Corneal Rings in Non-Wilsonian Liver Disease

  1. C. RICHARD FLEMING, M.D.;
  2. E. ROLLAND DICKSON, M.D., F.A.C.P.;
  3. HEINZ W. WAHNER, M.D.;
  4. ROBERT W. HOLLENHORST, M.D.; and
  5. JOHN T. McCALL, Ph.D.
  1. Rochester, Minnesota

    Abstract

    Kayser-Fleischer rings are pigmented corneal rings at the limbus of the cornea in Descemets membrane that have been deemed pathognomonic of Wilson's disease. However, we have observed four exceptions in patients with non-Wilsonian liver disease. Three patients had primary biliary cirrhosis and one patient had chronic aggressive hepatitis with cirrhosis. Pigmented corneal rings were seen only by slit-lamp examination. Hepatic, serum, and urinary copper and serum ceruloplasmin levels were significantly elevated in the patients with primary biliary cirrhosis. Radiocopper (64Cu or 67Cu) studies in patients with primary biliary cirrhosis showed plasma disappearance curves which allowed a clear distinction from Wilson's disease in that all three patients with primary biliary cirrhosis showed a secondary rise in radiocopper that presumably represented copper incorporation into ceruloplasmin. In one patient, in whom 64Cu in ceruloplasmin was studied specifically, incorporation was found to be normal.

    Article and Author Information

    • ▸ From Mayo Clinic; Rochester, Minnesota.

    • Grant support: Research Grant AM 19448-01 from the National Institute of Arthritis, Metabolism, and Digestive Diseases, National Institutes of Health; Bethesda, Maryland.

    • ▸ Requests for reprints should be addressed to C. Richard Fleming, M.D.; Mayo Clinic; Rochester, MN 55901.

      • Received July 9, 1976.
      • Accepted November 11, 1976.
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