Abstract
We here report a case of idiopathic hypereosinophilic syndrome with prompt response to treatment with imatinib. The patient presented with chest pain, myalgias, fatigue and weakness. Blood tests and bone marrow examination revealed striking eosinophilia. Clonal or reactive disorders were excluded by a wide range of diagnostic examinations. Treatment with high-dosis corticosteroids and hydroxyurea had little effect. Additional treatment with imatinib resulted in prompt symptomatic improvement and full haematological remission within five days of therapy.
Udgivelsesdato: 2008-Jan-21
Udgivelsesdato: 2008-Jan-21
Bidragets oversatte titel | Treatment of idiopathic hypereosinophilic syndrome with imatinib |
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Originalsprog | Dansk |
Tidsskrift | Ugeskrift for læger |
Vol/bind | 170 |
Udgave nummer | 4 |
Sider (fra-til) | 254 |
ISSN | 0041-5782 |
Status | Udgivet - 2008 |