Table 1.

Laboratory findings of 15 patients with pure red cell aplasia associated with lymphoproliferative disease of granular T lymphocytes

Median (range)Normal values
Hemoglobin (g/dL) 7.8  (5.0-10.5) 12.0-17.5  
Mean corpuscular volume (fL) 90  (83.0-117.9) 81.2-98.3  
White cell count (× 109/L) 6.6  (3.4-37.0) 3.5-10.5  
Absolute neutrophil count (× 109/L) 3.09  (0.12-5.41) 1.70-7.0  
Absolute lymphocyte count (× 109/L) 2.31  (1.06-29.97) 0.90-2.90 
Absolute granular lymphocyte count
(× 109/L) 
0.45  (0.30-7.21) 0.10-0.50  
Granular lymphocyte (%) 31  (10-59) 5-25 
Median (range)Normal values
Hemoglobin (g/dL) 7.8  (5.0-10.5) 12.0-17.5  
Mean corpuscular volume (fL) 90  (83.0-117.9) 81.2-98.3  
White cell count (× 109/L) 6.6  (3.4-37.0) 3.5-10.5  
Absolute neutrophil count (× 109/L) 3.09  (0.12-5.41) 1.70-7.0  
Absolute lymphocyte count (× 109/L) 2.31  (1.06-29.97) 0.90-2.90 
Absolute granular lymphocyte count
(× 109/L) 
0.45  (0.30-7.21) 0.10-0.50  
Granular lymphocyte (%) 31  (10-59) 5-25 

Clonal T-cell receptor gene rearrangement, 15 of 15 patients; positive direct antiglobulin test, 1 of 10 patients; positive antinuclear antibody test, 4 of 6 patients; rheumatoid factor, 1 of 4 patients; antineutrophil antibody, 0 of 2 patients. Cytogenetic studies, (n = 10 patients). Normal (8); loss of Y chromosome (1); complex abnormality (1). Peripheral blood flow cytometry, (n = 12 patients). CD3+/CD8+ (8); normal (4). Immunophenotypes studied include CD2, CD3, CD5, CD7, CD3/CD8, and CD3/CD4.

Bone marrow immunohistochemistry, (n = 9 patients). Increase in CD3+ and CD8+ cells (9); increase in CD57+ cells (8).

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