| Literature DB >> 15075087 |
Luca Malcovati, Roberta La Starza, Serena Merante, Daniela Pietra, Cristina Mecucci, Mario Cazzola.
Abstract
We studied a patient with hypereosinophilic syndrome (HES) who had myeloproliferative features, was unresponsive to imatinib mesylate, and showed cyclic oscillations in blood cell counts. No rearrangement in PDGFRA, PDGFRB and ETV6 genes was detected. Clonal analysis of hematopoiesis consistently showed skewed X-chromosome inactivation patterns in both granulocytes and T-lymphocytes, indicating a clonal myeloproliferative disorder originating in a pluripotent stem cell.Entities:
Mesh:
Year: 2004 PMID: 15075087
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941