| Literature DB >> 2500017 |
A Mijović1, Z Rolović, A Novak, L Biljanović-Paunović, D Tomin.
Abstract
After intermittent treatment with busulphan over a 7-year period for chronic myeloid leukemia (CML) in chronic phase, a 39-year-old female developed leukocytosis in association with pure red cell aplasia (PRCA). Bone marrow examination confirmed erythroid aplasia, and culture revealed a total absence of erythroid progenitor cells. The patient then was treated with azathioprine, corticosteroids, cyclophosphamide, plasma exchange, and cyclosporin A, but she remained erythroblastopenic and transfusion dependent for more than a year, at which time a promyelocytic transformation supervened. The authors propose that this sequence of events, hitherto unreported, is a manifestation of the multistep progression of CML.Entities:
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Year: 1989 PMID: 2500017 DOI: 10.1002/ajh.2830310211
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047