Primary Biliary Cirrhosis and Hemolytic Anemia Confusing Serum Bilirubin Levels
Author(s) -
Muriel Brackstone,
Cameron N. Ghent
Publication year - 2000
Publication title -
canadian journal of gastroenterology
Language(s) - English
Resource type - Journals
eISSN - 1916-7237
pISSN - 0835-7900
DOI - 10.1155/2000/148063
Subject(s) - primary biliary cirrhosis , hemolysis , medicine , hemolytic anemia , autoimmune hemolytic anemia , gastroenterology , biliary cirrhosis , anemia , cirrhosis , hereditary spherocytosis , context (archaeology) , liver transplantation , immunology , transplantation , disease , autoimmune disease , paleontology , biology
Hemolysis is observed in more than 50% of patients with cirrhosis. However, there has been little documentation of the association of primary biliary cirrhosis with autoimmune hemolytic anemia. Two cases, found within a single practice, of primary biliary cirrhosis coexisting with autoimmune hemolysis and a third case coexisting with hereditary spherocytosis are presented. Anemia in such patients is commonly attributed to chronic disease, and hyperbilirubinemia is attributed to primary biliary cirrhosis. These patients were considered for liver transplantation until the diagnosis of a comorbid hemolytic process was established. This association may be more prevalent than previously recognized. A diagnosis of comorbid hemolysis must always be considered in context with anemia and serum bilirubin levels that rise out of proportion to the severity of the primary biliary cirrhosis.
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