Abstract
Hypereosinophilia is a rare presenting sign of acute lymphocytic leukemia. A 29-year-old male was diagnosed with idiopathic hypereosinophilic syndrome with respiratory symptoms. Although his peripheral blood eosinophilia decreased in response to treatment with imatinib mesylate, a follow-up bone marrow showed a diffuse infiltrate of myeloperoxidase-negative blasts. He was subsequently diagnosed with CD10 positive precursor B lymphoblastic leukemia. This case underscores the importance of follow-up bone marrow examination in patients who demonstrate imatinib mesylate-responsive eosinophilia.
Original language | English (US) |
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Pages (from-to) | 2497-2501 |
Number of pages | 5 |
Journal | Leukemia and Lymphoma |
Volume | 45 |
Issue number | 12 |
DOIs | |
State | Published - Dec 2004 |
Keywords
- ALL/Eo
- Hypereosinophilic syndrome
- Imatinib mesylate
ASJC Scopus subject areas
- Hematology
- Oncology
- Cancer Research