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Fulminant Wilson disease

Fulminant Wilson disease
#00014406
Author: Michael H. Rosove and Neeharika Srivastava
Category: Underproduction Anemias
Published Date: 12/09/2012

A 37-year-old woman with no previous medical problems noted malaise, jaundice, and dark urine that rapidly progressed to severe liver failure. She was referred for an evaluation of anemia. Her hemoglobin was 7.3 g/dL, reticulocyte count 132 000/µL, bilirubin 29.6 mg/dL, lactate dehydrogenase 1834 U/L, and alanine aminotransferase was normal. The blood smear revealed marked spherocytosis, “spur” cells, polychromasia, and nucleated red blood cells (panel A). The serum haptoglobin was undetectable and the direct antiglobulin (Coombs) test was negative. A serum ceruloplasmin was 20 mg/dL (normal, 18-54 mg/dL). The combination of the peripheral smear and evidence of hemolysis with liver failure made Wilson disease a strong consideration. An examination of her eyes revealed Kaiser-Fleischer (KF) rings. Emergency liver transplantation was performed. Her preoperative 24-hour urine later returned showing 2760 µg copper (normal, 3-50 µg).