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- W2034159648 abstract "The classical myeloproliferative neoplasms (MPNs) feature an overproduction of mature blood elements. Phenotypic conversion, including transformation to myelofibrosis (MF) in those with antecedent ET and PV is a feared complication. Hypereosinophilic syndromes (HESs), especially those with myeloproliferative variants, can display similar features, including organomegaly, marrow fibrosis, clonality, thrombotic tendencies, and acute myeloid leukemia (AML) transformation. However, this group of illnesses is typically clinically and molecularly distinct from the classical MPNs. We report a case of a 59-yr-old woman with complex hypereosinophilia in the setting of post-polycythemic myelofibrosis (post-PVMF), with multi-system end-organ damage characteristic of HES." @default.
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- W2034159648 date "2012-01-01" @default.
- W2034159648 modified "2023-09-27" @default.
- W2034159648 title "Complex hypereosinophilia arising from post-polycythemia vera myelofibrosis: A case of imatinib-responsiveness" @default.
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- W2034159648 doi "https://doi.org/10.1016/j.lrr.2012.07.001" @default.
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