Successful treatment of acquired amegakaryocytic thrombocytopenic purpura refractory to corticosteroids and intravenous immunoglobulin with antithymocyte globulin and cyclosporin

Author:

Niparuck Pimjai,Atichartakarn Vichai,Chuncharunee Suporn

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Reference19 articles.

1. Hoffman R. Acquired pure amegakaryocytic thrombocytopenic purpura. Semin Hematol. 1991;28:303–12.

2. Gewirtz AM, Hoffman R. Primary platelet production disorders. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al., editors. Hematology: basic principles and practice. New York: Churchill-Livingstone; 1991. p. 205–10.

3. Rovira M, Feliu E, Florensa L. Acquired amegakaryocytic thrombocytopenic purpura associated with immunoglobulin deficiency. Acta Haematol. 1991;85:34–6.

4. Erkurt MA, Kaya E, Baran M, Yitmen E, Fienel S, Kuku L, et al. Rapid progression of acquired amegakaryocytic thrombocytopenia to myelodysplastic syndrome: case report. Turk J Haematol. 2005;22(4):205–8.

5. Griner PH, Hoyer LW. Amegakaryocytic thrombocytopenia in systemic lupus erythematosus. Arch Int Med. 1970;125:328–32.

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