Table 1

Clinical and laboratory characteristics of monoclonal TCRαβ+/CD4+ LGL lymphocytosis according to the type of TCR-Vβ family expressed (Vβ13.1 versus non-Vβ13.1) compared with monoclonal TCRαβ+/CD8+ LGL lymphocytosis

CharacteristicMonoclonal TCRαβ+/CD4+ LGL lymphocytosis
Monoclonal TCRαβ+/CD8+ LGL lymphocytosisP
TCR-Vβ13.1Non-TCR-Vβ13.1Total cases
No. of patients 15 21 36 24  
Mean age ± 1 SD, y (range) 64 ± 8 (52-80) 61 ± 13 (36-81) 63 ± 12 (36-81) 56 ± 15 (31-79) NS 
% male/% female 25/75 61/39 47/53 37/63 NS 
Reason for consulting, %
    Routine blood analysis 100 83 90 83 NS 
    Skin lesions 11 NS 
    Abdominal distension NS 
    Fever NS 
    General symptoms 13 NS 
Physical examination, %
    Adenomegalies 11 NS 
    Hepatomegaly NS 
    Splenomegaly NS 
    Skin lesions 11 NS 
Associated neoplasias, % 25 22 23 26 NS 
Associated autoimmune diseases, % 18 13 33 .05 
Laboratory parameters, %
    Leukocytosis, WBC count more than 10 × 109/L 64 61 63 25 .01 
    Lymphocytosis, lymphocyte count more than 5 × 109/L 70 67 68 42 .09 
    Neutropenia, neutrophil count less than 1.5 × 109/L 14 61 < .001 
    Anemia, hemoglobin level less than 10 g/dL 29 .003 
    Thrombocytopenia, platelet count less than 100 × 109/L 10 NS 
    Increased lactic dehydrogenase level, more than 460 U/L 10 22 NS 
    Increased β2-microglobulin level, more than 2 mg/dL 63 .001 
Cases requiring treatment because of lymphocytosis or the associated autoimmune disease, % 37 .001 
Outcome: stable disease, % 100 100 100 87 NS 
Total deaths, % 10 18 15 NS 
Deaths related to the TCRαβ+ LGL lymphocytosis, % NS 
Mean follow-up ± 1 SD, mo (range) 68 ± 48 (13-136) 74 ± 56 (10-233) 72 ± 53 (10-233) 44 ± 40 (1-152) .03 
CharacteristicMonoclonal TCRαβ+/CD4+ LGL lymphocytosis
Monoclonal TCRαβ+/CD8+ LGL lymphocytosisP
TCR-Vβ13.1Non-TCR-Vβ13.1Total cases
No. of patients 15 21 36 24  
Mean age ± 1 SD, y (range) 64 ± 8 (52-80) 61 ± 13 (36-81) 63 ± 12 (36-81) 56 ± 15 (31-79) NS 
% male/% female 25/75 61/39 47/53 37/63 NS 
Reason for consulting, %
    Routine blood analysis 100 83 90 83 NS 
    Skin lesions 11 NS 
    Abdominal distension NS 
    Fever NS 
    General symptoms 13 NS 
Physical examination, %
    Adenomegalies 11 NS 
    Hepatomegaly NS 
    Splenomegaly NS 
    Skin lesions 11 NS 
Associated neoplasias, % 25 22 23 26 NS 
Associated autoimmune diseases, % 18 13 33 .05 
Laboratory parameters, %
    Leukocytosis, WBC count more than 10 × 109/L 64 61 63 25 .01 
    Lymphocytosis, lymphocyte count more than 5 × 109/L 70 67 68 42 .09 
    Neutropenia, neutrophil count less than 1.5 × 109/L 14 61 < .001 
    Anemia, hemoglobin level less than 10 g/dL 29 .003 
    Thrombocytopenia, platelet count less than 100 × 109/L 10 NS 
    Increased lactic dehydrogenase level, more than 460 U/L 10 22 NS 
    Increased β2-microglobulin level, more than 2 mg/dL 63 .001 
Cases requiring treatment because of lymphocytosis or the associated autoimmune disease, % 37 .001 
Outcome: stable disease, % 100 100 100 87 NS 
Total deaths, % 10 18 15 NS 
Deaths related to the TCRαβ+ LGL lymphocytosis, % NS 
Mean follow-up ± 1 SD, mo (range) 68 ± 48 (13-136) 74 ± 56 (10-233) 72 ± 53 (10-233) 44 ± 40 (1-152) .03 

P value corresponds to comparisons between monoclonal TCRαβ+/CD4+ LGL and TCRαβ+/CD8+ LGL lymphocytosis; NS indicates no statistically significant differences: P > .1. No statistically significant differences (P > .05) were found between TCR-Vβ13.1 and non-TCR-Vβ13.1 clonal CD4+ LGL lymphocytosis. A detailed description of the clinical characteristics of patients with monoclonal TCRαβ+/CD4+ LGL lymphocytosis is provided by Lima et al.18 

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