| Literature DB >> 17696202 |
Paul R Yenson1, Donna Forrest, Kjell Schmiegelow, Bakul I Dalal.
Abstract
Immunosuppressive thiopurines like azathioprine, 6-mercaptopurine, and thioguanine are commonly used in inflammatory and neoplastic disorders. A subset of these patients are genetically slow metabolizers due to point-mutations in enzyme thiopurine S-methyltransferase (TPMT), and are at a higher risk of hematologic toxicity and leukemogenesis. We present such a patient who was a slow metabolizer for azathioprine, and developed a rapidly lethal form acute myeloid leukemia after relatively low dose exposure to the drug. There was prominent hemophagocytic activity in the bone marrow, and cytogenetic analysis showed a complex karyotype with monosomy 7, but no involvement of chromosome 8.Entities:
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Year: 2008 PMID: 17696202 DOI: 10.1002/ajh.21014
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047