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.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | American Journal of Hematology |
| Vol/bind | 83 |
| Udgave nummer | 1 |
| Sider (fra-til) | 80-3 |
| Antal sider | 4 |
| ISSN | 0361-8609 |
| DOI | |
| Status | Udgivet - jan. 2008 |
Fingeraftryk
Dyk ned i forskningsemnerne om 'Azathioprine-associated acute myeloid leukemia in a patient with Crohn's disease and thiopurine S-methyltransferase deficiency'. Sammen danner de et unikt fingeraftryk.Citationsformater
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