A 66-year-old male patient with severe intravascular hemolysis is presented
. Laboratory investigation revealed initially a negative direct antiglobuli
n test (DAT), suggesting a Coombs-negative hemolytic anemia, Additional tes
ting with monospecific anti-IgA was strongly positive. IgA autoantibodies w
ith anti-e specificity and nonspecific IgA autoantibodies were identified.
A diagnosis of IgA-only-associated warm AIHA was made. Treatment included t
ransfusion of multiple e-negative typed red cell concentrates and administr
ation of high-dose prednisone. The pathophysiologic mechanism of the rare I
gA-induced warm AIHA is discussed. (C) 2001 Elsevier Science B.V. All right
s reserved.