| Literature DB >> 18024388 |
G Helbig1, B Stella-Holowiecka, M Majewski, M Lewandowska, J Holowiecki.
Abstract
The JAK2 V617F point mutation is very rare in hypereosinophilic syndrome and/or chronic eosinophilic leukemia. Here we report on a patient with chronic eosinophilic leukemia and detectable JAK2 mutant clone, who achieved a good molecular response to interferon alpha-2a after 4 months of treatment. The molecular response correlated with only moderate haematological improvement.Entities:
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Year: 2007 PMID: 18024388 DOI: 10.3324/haematol.11841
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941