Table 4.

Clinical and pathologic features of patients with MDS, MDS/MPD, or AML positive for JAK2 V617F mutation









Bone marrow morphology




WHO diagnosis
Age
Hgb, g/L
Platelets, × 109/L
MCV, fL
ANC, ×109/L
AMC, ×109/L
Blasts, %
Cellularity, %
Megakaryocytes
Megakaryocyte morphology
Reticulin fibrosis
RS, %
Cytogenetics
IPSS score
Splenomegaly, Y/N
JAK2 V617F mutation
RAEB-2   82   114   7   86.3   1.278   0.711   9*  10   Decreased   Dysplastic, small, hyposegmented   3+   2   NA—no growth 43-45,XX,del(5)(q13q33), -6,-10,-13,add(17) (p11.2),-20,+r, +1-3mar[cp7]/46,XX[13]   1   Y   G/T  
AML   75   108   18   94.3   2.369   0.115   24   70   Decreased   Normal   2+   4    2   N   G/T  
CMML-1   79   113   309   94.7   6.170   1.199   0   85   Increased and clustered   Large, complex hyperlobate nuclei   2+   2   47,XY,+8[7]/46,XY[13]   0.5   N   G/T  
CMML-2   44   89   499   86.1   24.078   7.223   9  100   Increased and clustered   Dysplastic   3+   1   46,XY,t(8;9)(q22;p24)[20]   1   Y   G/T  
MDS/MPD-U§  79   96   122   90.9   4.328   0.108   0   30  Increased and clustered   Dysplastic hyperchromatic nuclei   4+  65   46,XX[20]   0.5   Y   G/T  
MDS/MPD-U§  71   83   413   89.8   6.578   0   7   30  Increased, focally clustered   Dysplastic hyperchromatic nuclei   4+  0   47,XY,+8[14]   1   Y   G/T  
MDS/MPD-U§
 
63
 
85
 
8
 
95.3
 
5.852
 
0.228
 
2
 
10
 
Decreased
 
Dysplastic, hyperchromatic hyposegmented nuclei
 
3+
 
0
 
NA-no growth
 
0.5
 
Y
 
G/T
 








Bone marrow morphology




WHO diagnosis
Age
Hgb, g/L
Platelets, × 109/L
MCV, fL
ANC, ×109/L
AMC, ×109/L
Blasts, %
Cellularity, %
Megakaryocytes
Megakaryocyte morphology
Reticulin fibrosis
RS, %
Cytogenetics
IPSS score
Splenomegaly, Y/N
JAK2 V617F mutation
RAEB-2   82   114   7   86.3   1.278   0.711   9*  10   Decreased   Dysplastic, small, hyposegmented   3+   2   NA—no growth 43-45,XX,del(5)(q13q33), -6,-10,-13,add(17) (p11.2),-20,+r, +1-3mar[cp7]/46,XX[13]   1   Y   G/T  
AML   75   108   18   94.3   2.369   0.115   24   70   Decreased   Normal   2+   4    2   N   G/T  
CMML-1   79   113   309   94.7   6.170   1.199   0   85   Increased and clustered   Large, complex hyperlobate nuclei   2+   2   47,XY,+8[7]/46,XY[13]   0.5   N   G/T  
CMML-2   44   89   499   86.1   24.078   7.223   9  100   Increased and clustered   Dysplastic   3+   1   46,XY,t(8;9)(q22;p24)[20]   1   Y   G/T  
MDS/MPD-U§  79   96   122   90.9   4.328   0.108   0   30  Increased and clustered   Dysplastic hyperchromatic nuclei   4+  65   46,XX[20]   0.5   Y   G/T  
MDS/MPD-U§  71   83   413   89.8   6.578   0   7   30  Increased, focally clustered   Dysplastic hyperchromatic nuclei   4+  0   47,XY,+8[14]   1   Y   G/T  
MDS/MPD-U§
 
63
 
85
 
8
 
95.3
 
5.852
 
0.228
 
2
 
10
 
Decreased
 
Dysplastic, hyperchromatic hyposegmented nuclei
 
3+
 
0
 
NA-no growth
 
0.5
 
Y
 
G/T
 

MDS indicates myelodysplastic syndrome; MDS/MPD, myelodysplastic/myeloproliferative disease; AML, acute myeloid leukemia; RAEB, refractory anemia with excess blasts; CMML, chronic myelomonocytic leukemia; MCV, mean cell volume; ANC, absolute neutrophil count; AMC, absolute monocyte count; RS, ringed sideroblasts; and NA, not available.

*

10% blasts in peripheral blood.

12% blasts in peripheral blood.

Extensive reticulin and collagenous stromal fibrosis.

§

Cases of MDS/MPD-U classified as RARS-T were excluded and presented in a separate table (Table 3).

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