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Amegakaryocytic thrombocytopenia of 4 years duration: successful treatment with antithymocyte globulin
M S Trimble1, M F Glynn, M C Brain
1Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
American Journal of Hematology
|June 1, 1991
Abstract:
Acquired amegakaryocytic thrombocytopenic purpura (AATP) is a rare cause of thrombocytopenia. Since it is a syndrome of diverse etiologies, the optimal treatment is often uncertain. In a patient with longstanding AATP, a complete remission was obtained with antithymocyte globulin.
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