Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10897647 | Cancer Genetics | 2012 | 4 Pages |
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.
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Authors
Anas Alrwas, Jorge R. Quesada, Luis A. Marcos, Shivang S. Mehta, Brandy L. Shattuck, Nghia D. Nguyen, Harinder S. Juneja,