Abstract
We report an unusual case of a symptomatic patient who initially had high hemoglobin and low serum erythropoietin levels, fitting a clinical diagnosis of polycythemia vera. However, after treatment with hydroxyurea and serial phlebotomies had been started, the patient developed hypereosinophilia, fitting the category of a myeloproliferative neoplasm with eosinophilia associated with the FIP1L1-PDGFRA gene fusion, as confirmed by molecular analysis. We discuss the clinical presentation, evolution, response to treatment, and pathogenetic implications of this case.
| Original language | English |
|---|---|
| Pages (from-to) | 519-522 |
| Number of pages | 4 |
| Journal | Cancer Genetics |
| Volume | 205 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 2012 |
Keywords
- Chronic myeloproliferative neoplasms
- Concurrent
- Hypereosonophilia
- Polycythemia vera
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