Abstract
We report a 49-year-old man suffering from chronic hypereosinophilia whose biological tests revealed a gene rearrangement between FIP1L1 and PDGFRA as well as a T-cell clonality. After 1 year of therapy with imatinib mesylate (100 mg daily), the patient was clinically asymptomatic, the fusion transcript was undetectable using RTQ-PCR and no lymphoproliferative disorders occurred. This unique combination raises the question of the physiopathology of such a grey zone hypereosinophilia and their management.
Copyright © 2010. Published by Elsevier SAS.
Publication types
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Case Reports
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English Abstract
MeSH terms
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Antineoplastic Agents / therapeutic use
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Benzamides
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Chronic Disease
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Gene Rearrangement, T-Lymphocyte / genetics
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Genetic Testing
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Humans
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Hypereosinophilic Syndrome / drug therapy
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Hypereosinophilic Syndrome / genetics*
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Hypereosinophilic Syndrome / pathology*
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Imatinib Mesylate
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Male
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Middle Aged
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Mutation / genetics*
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Oncogene Proteins, Fusion / genetics*
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Piperazines / therapeutic use
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Pyrimidines / therapeutic use
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Receptor, Platelet-Derived Growth Factor alpha / genetics*
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T-Lymphocytes / pathology*
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Treatment Outcome
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mRNA Cleavage and Polyadenylation Factors / genetics*
Substances
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Antineoplastic Agents
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Benzamides
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FIP1L1 protein, human
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Oncogene Proteins, Fusion
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Piperazines
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Pyrimidines
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mRNA Cleavage and Polyadenylation Factors
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Imatinib Mesylate
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Receptor, Platelet-Derived Growth Factor alpha