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Leukemia ; 25(9): 1439-43, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21617700

ABSTRACT

T-cell large granular lymphocytic (LGL) leukemia is a complex diagnosis, requiring persistent clonal expansions of LGLs, and cytopenias. Often the diagnosis is unclear as non-clonal expansions of LGLs commonly occur in reactive conditions. To better understand T-LGL leukemia, we performed a comprehensive clinicopathologic analysis of 85 patients with LGL expansions. Interestingly, distinct CD8+(dim)/CD57+ populations, seen by flow cytometry, were significantly associated with clonal T-LGL leukemia (P < 0.001) as well as neutropenia (median absolute neutrophil count (ANC) 1.45 vs 3.19 × 10(9)/l; P = 0.0017). Furthermore, cases with distinct CD8+(dim)/CD57+ populations and monoclonal T cells had even lower ANCs (median ANC 1.41 × 10(9)/l; P = 0.001) compared with cases without these dual criteria. Additionally, complete or partial loss of CD5 expression was independently associated with clonal T-LGL leukemia (P<0.001) and neutropenia (median ANC 1.41 vs 2.70 × 10(9)/l; P = 0.002). This study describes specific immunophenotypic parameters to better define clonal cases of T-LGL leukemia associated with significant neutropenia.


Subject(s)
Leukemia, Large Granular Lymphocytic/diagnosis , Leukemia, Large Granular Lymphocytic/metabolism , Receptors, Antigen, T-Cell, alpha-beta/metabolism , T-Lymphocytes/metabolism , Adult , Aged , Aged, 80 and over , Clone Cells , Female , Flow Cytometry , Gene Rearrangement, beta-Chain T-Cell Antigen Receptor/genetics , Gene Rearrangement, beta-Chain T-Cell Antigen Receptor/immunology , Humans , Immune System/immunology , Immunophenotyping , Inflammation/diagnosis , Inflammation/immunology , Inflammation/metabolism , Leukemia, Large Granular Lymphocytic/immunology , Male , Middle Aged , Neutropenia/diagnosis , Neutropenia/immunology , Neutropenia/metabolism , Receptors, Antigen, T-Cell, alpha-beta/genetics , T-Lymphocytes/immunology , Young Adult
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