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.

journal_name

Am J Hematol

authors

Leach JW,Hussein KK,George JN

doi

10.1002/(sici)1096-8652(199910)62:2<115::aid-ajh10

keywords:

subject

Has Abstract

pub_date

1999-10-01 00:00:00

pages

115-7

issue

2

eissn

0361-8609

issn

1096-8652

pii

10.1002/(SICI)1096-8652(199910)62:2<115::AID-AJH10

journal_volume

62

pub_type

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