Abstract
We report the emergence of chronic myelogenous leukemia (CML) in a patient with JAK2V617F-positive polycythemia vera after 15 years of phlebotomy. The polycythemia vera clinical and molecular findings were suppressed at the time of CML diagnosis, only to re-emerge after the leukemia was successfully treated with imatinib. We explored the potential association between myeloproliferative disorders and CML in the context of the current literature and found a higher-than-expected coincidence based on known epidemiologic data for each specific condition. We hypothesize that myeloproliferative disorder (JAK2V617F or molecular events that cause JAK2V617F) is a risk factor for CML (BCR-ABL translocation). Because of therapeutic implications, clinicians should be aware that the conditions co-occur more frequently than once thought.
Original language | English (US) |
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Pages (from-to) | E25-9 |
Journal | Clinical Lymphoma and Myeloma |
Volume | 9 |
Issue number | 5 |
DOIs | |
State | Published - Oct 2009 |
Keywords
- Adult
- Fusion Proteins, bcr-abl
- Humans
- Janus Kinase 2
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
- Male
- Myeloproliferative Disorders
- Phlebotomy
- Risk Factors
- Translocation, Genetic
- Case Reports
- Journal Article
- Research Support, Non-U.S. Gov't