Acquired pure megakaryocytic aplasia report of two cases with long-term responses to antithymocyte globulin and cyclosporine.

Abstract

Acquired pure megakaryocytic aplasia is a rare disorder defined by severe thrombocytopenia with no other hematologic abnormalities and absent, or severely decreased marrow megakaryocytes. The etiology may be immune suppression of megakaryocyte development. Two patients are described who both responded rapidly to a combination of antithymocyte globulin and cyclosporine and who remain in remission 13-20 months after discontinuation of cyclosporine. This regimen is well described for treatment of aplastic anemia and may also be effective for acquired pure megakaryocytic aplasia.

• Authors: J W Leach, K K Hussein, J N George
• Journal: American journal of hematology (Am J Hematol) Vol. 62 Issue 2 Pg. 115-7 (Oct 1999) ISSN: 0361-8609 [Print] United States
• PMID: 10577280 (Publication Type: Case Reports, Journal Article)

Chemical References

• Antilymphocyte Serum
• Immunosuppressive Agents
• Cyclosporine
• Prednisone

Topics

• Adult
• Antilymphocyte Serum (therapeutic use)
• Cyclosporine (therapeutic use)
• Drug Therapy, Combination
• Female
• Humans
• Immunosuppressive Agents (therapeutic use)
• Indians, North American
• Male
• Megakaryocytes (pathology)
• Middle Aged
• Oklahoma
• Prednisone (therapeutic use)
• Thrombocytopenia (blood, drug therapy, pathology)
• Time Factors