Table 1.

Patients recruited to the study


Patient

Age, y/sex

History of aplastic anemia*

Thrombosis

Hemoglobin level, g/dL

Reticulocyte count, %

WBC count, × 109/L

Platelet count, × 109/L

% PNH III red blood cells

% PNH II red blood cells

% PNH polymorphonuclear leukocytes

Treatment
1   29/F   Yes   No   5.4   2.6   2.5   19   20   5   70   ATG  
2   51/M   Yes   No   9.7   —   —   100   9   24   74   ATG/CSA  
3   40/F   No   Yes   12.4   2.2   4.2   74   6   6   52   Enoxaparin  
4   74/M   No   No   9.9   8.1   3.4   92   34   9   84   Transfusion  
5
 
33/F
 
No
 
No
 
9.4
 
20.2
 
3.7
 
263
 
28
 
24
 
83
 
Transfusion
 

Patient

Age, y/sex

History of aplastic anemia*

Thrombosis

Hemoglobin level, g/dL

Reticulocyte count, %

WBC count, × 109/L

Platelet count, × 109/L

% PNH III red blood cells

% PNH II red blood cells

% PNH polymorphonuclear leukocytes

Treatment
1   29/F   Yes   No   5.4   2.6   2.5   19   20   5   70   ATG  
2   51/M   Yes   No   9.7   —   —   100   9   24   74   ATG/CSA  
3   40/F   No   Yes   12.4   2.2   4.2   74   6   6   52   Enoxaparin  
4   74/M   No   No   9.9   8.1   3.4   92   34   9   84   Transfusion  
5
 
33/F
 
No
 
No
 
9.4
 
20.2
 
3.7
 
263
 
28
 
24
 
83
 
Transfusion
 

To convert hemoglobin level from grams per deciliter to grams per liter, multiply grams per deciliter by 10.

ATG indicates equine antithymocyte globulin; WBC, white blood cell; CSA, cyclosporine; and —, not available.

*

Prior or concurrent history of clinically recognized aplastic anemia.

Fraction of PNH red cells and granulocytes was performed as previously described.25 

Red cells with a partial deficiency in CD59 expression.

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