Table 1.

Percentage of abnormal nuclei in each cell lineage of 4 patients with myelofibrosis with myeloid metaplasia studied with fluorescent in situ hybridization using probes to detect 13q− and 20q−

PatientCD3+CD19+PMNCD34+CD61+CD71+
1 del(13)(q12q21.2) in 20 of 20 metaphases 42 61 82 58 75 78  
2 del(13)(q12q14) in 20 of 20 metaphases 13 90 51 94 88  
3 del(20)(q13.1) in 20 of 20 metaphases 57 96 98 87 77 81  
4 del(20)(q13.1) in 16 of 21 metaphases 21 30 86 36 67 57 
PatientCD3+CD19+PMNCD34+CD61+CD71+
1 del(13)(q12q21.2) in 20 of 20 metaphases 42 61 82 58 75 78  
2 del(13)(q12q14) in 20 of 20 metaphases 13 90 51 94 88  
3 del(20)(q13.1) in 20 of 20 metaphases 57 96 98 87 77 81  
4 del(20)(q13.1) in 16 of 21 metaphases 21 30 86 36 67 57 

Each column represents T cells (CD3+), B cells (CD19+), neutrophils (PMN), myeloid progenitor cells (CD34+), megakaryocyte precursor cells (CD61+), and erythroid cells (CD71+). Normal ranges are < 9.5% for 13q− and < 11.5% for 20q−.

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