Table 4.

FISH Results Using Centromeric Probes in 13 Primary PCL Cases and 56 MM Cases

Chromosome PCL Patients (n = 13) MM Patients (n = 56)
MonosomyTrisomy Monosomy Trisomy
 1  14%  43%  3% 37%  
 3  0%  0%  0%  31%  
 64-150 0% 0%  0%  32%  
 7  0%  0%  0%  28% 
 8  0%  0%  5%  8%  
 94-150 0%  0% 0%  52%  
10  0%  0%  0%  8%  
11  0% 0%  3%  33%  
12  0%  0%  0%  3%  
134-150 86%  0%  26%  0%  
15  0%  0%  0% 48%  
17  0%  0%  0%  22%  
18  0% 43%  6%  24%  
X  25%4-151 0%  32%4-151 6% 
Y  0%  0%  0%  0% 
Chromosome PCL Patients (n = 13) MM Patients (n = 56)
MonosomyTrisomy Monosomy Trisomy
 1  14%  43%  3% 37%  
 3  0%  0%  0%  31%  
 64-150 0% 0%  0%  32%  
 7  0%  0%  0%  28% 
 8  0%  0%  5%  8%  
 94-150 0%  0% 0%  52%  
10  0%  0%  0%  8%  
11  0% 0%  3%  33%  
12  0%  0%  0%  3%  
134-150 86%  0%  26%  0%  
15  0%  0%  0% 48%  
17  0%  0%  0%  22%  
18  0% 43%  6%  24%  
X  25%4-151 0%  32%4-151 6% 
Y  0%  0%  0%  0% 

Results are expressed as a percentage of trisomic/monosomic cases for MM patients.

F4-150

Chromosomes in which the incidence of numeric aberrations was different between PCL and MM (P < .05).

F4-151

Calculated only in females (0% in males).

Calculated only in males (0% in females).

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