Abstract
A patient with familial erythrocytosis associated with Hemoglobin Rainier, and previously treated with 32P, developed myelofibrosis with a hyperdiploid chromosome clone in the myeloid cells (51, XX, +1, 2q‐(q33), +6, +9, +11, ‐19, +20q +,+ mar 1). This transformation from a benign disorder of differentiated erythrocytes to a malignant disorder may have been secondary to radiophosphorus therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 63-69 |
| Number of pages | 7 |
| Journal | American Journal of Hematology |
| Volume | 5 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1978 |
| Externally published | Yes |
Keywords
- Hemoglobin Rainier
- P
- chromosome 1, 6, 9, and 11 aberrations
- cytogenetics
- hematology
- hemoglobinopathy
- myelofibrosis
- myeloproliferative disorder
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