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An unusual case of autoimmune hemolytic anemia with reticulocytopenia, erythroid dysplasia, and an IgG2 autoanti‐U
Author(s) -
Roush G. R.,
Rosenthal N. S.,
Gerson S. L.,
Toy E. M.,
McCarthy P.,
Hirschler N. V.,
Yomtovian R.
Publication year - 1996
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1046/j.1537-2995.1996.36696269519.x
Subject(s) - hematocrit , medicine , hemolysis , autoimmune hemolytic anemia , hemolytic anemia , coombs test , anemia , autoantibody , immunology , bone marrow , gastroenterology , antibody
BACKGROUND: Autoantibodies with anti‐U specificity, usually in combination with autoantibodies of other specificities, have occasionally been identified in association with autoimmune hemolytic anemia. A case of life‐threatening autoimmune hemolytic anemia, characterized by several atypical features, including apparent intravascular hemolysis associated with an IgG2 anti‐U, reticulocytopenia, and bone marrow dyserythropoiesis is described. CASE REPORT: A 36‐year‐old man with a severe case of acute‐onset autoimmune hemolytic anemia was admitted to another hospital; he had a hematocrit of 15 percent, elevated bilirubin and lactate dehydrogenase, and positive direct and indirect antiglobulin tests. He received 7 units of incompatible red cells without improvement in hematocrit, and he was transferred to University Hospitals of Cleveland (OH). He was jaundiced and became syncopal in the sitting position. His serum was reddish pink; he had a hematocrit of 11.8 percent and a reticulocyte count of 2.5 percent. No spherocytes were observed in the peripheral blood smear. Shortly after admission, the hematocrit fell to 6.9 percent. He was given 3 units of “least‐incompatible” red cells and was started on prednisone, with little improvement. An IgG2 autoanti‐U was detected in his serum. Seven units of U‐ red cells were transfused over the next 4 days. The hematocrit improved to 23 percent and continued to rise without further transfusion. A bone marrow examination, initially revealing erythroid hyperplasia accompanied by dyserythropoiesis, became morphologically normal. Drug studies failed to show evidence of drug‐related hemolysis. He remains well 2 years after discharge without evidence of recurrent hemolysis. CONCLUSION: Severe life‐threatening autoimmune hemolytic anemia, in this instance induced by an autoanti‐U, may be associated with IgG2 autoantibody and characterized by apparent intravascular hemolysis and bone marrow dyserythropoiesis. Early treatment with U‐ blood, in addition to steroids, may be beneficial.