| Literature DB >> 18036706 |
S Menif1, N Ben Romdhane, R Hafsia.
Abstract
Hypereosinophilic syndromes (HES) are a heterogeneous group of disorders characterized by marked peripheral blood and tissue eosinophilia resulting in organ damage. Recent advances in molecular biology have led to the identification of a FIP1L1-PDGFRA fusion gene as a recurrent abnormality in some patients with HES. This fusion gene results from a cryptic 4q12 interstitial deletion involving an 800 kb region. Recent reports indicate that this subtype of HES is imatinib responsive with rapid and complete haematological remissions. Here we report two patients successfully treated with imatinib.Entities:
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Year: 2007 PMID: 18036706 DOI: 10.1016/j.revmed.2007.09.036
Source DB: PubMed Journal: Rev Med Interne ISSN: 0248-8663 Impact factor: 0.728