Abstract
Hypereosinophilic syndrome (HES) is a disease process of unknown pathogenesis. Although some cases are believed to be primary hematologic malignancies, this issue remains unsolved. We present a case of HES in whom we have observed a clone of cytogenetically abnormal cells in the bone marrow in parallel with a clinical picture of a hematologic disorder characterized by progressive proliferation and organ infiltration by eosinophils. The cytogenetic abnormality 46,XY,t(7;12)(q11;p11) is previously unreported. Our case, plus other evidence present in the literature, supports the concept that HES is a hematologic malignant neoplasia.
| Original language | English |
|---|---|
| Pages (from-to) | 109-115 |
| Number of pages | 7 |
| Journal | Cancer Genetics and Cytogenetics |
| Volume | 32 |
| Issue number | 1 |
| DOIs | |
| State | Published - May 1988 |
| Externally published | Yes |
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