Large granular lymphocytic leukemias (LGLLs) are a heterogeneous group of rare chronic lymphoproliferative disorders characterized by the clonal proliferation of cytotoxic lymphocytes. Among them, T-cell LGLL (T-LGLL) and NK-cell LGLL (NK-LGLL) are the most prominent. Due to overlapping morphological, clinical, and immunophenotypic characteristics, distinguishing these disorders from related entities such as T-prolymphocytic leukemia (T-PLL), adult T-cell leukemia/lymphoma (ATLL), Sézary syndrome (SS), and aggressive NK-cell leukemia (ANKL) presents a significant diagnostic challenge. This review integrates recent molecular insights and updates from the WHO 5th edition classification to refine diagnostic precision and inform individualized patient management strategies.
T-cell Large Granular Lymphocytic Leukemia (T-LGLL)
T-LGLL presents with chronic neutropenia, anemia, and autoimmune phenomena—most notably rheumatoid arthritis. Morphologically, cells are small to medium-sized with azurophilic granules. Immunophenotyping reveals a CD8+ cytotoxic profile with frequent expression of CD57, CD16, and granzyme markers. A defining molecular feature is the presence of STAT3 mutations, with STAT5B mutations occasionally observed in CD4+ variants. Clonality is confirmed by T-cell receptor (TCR) gene rearrangement. The WHO's updated diagnostic criteria emphasize increased circulating cytotoxic T cells, aberrant immunophenotype, and TCR monoclonality, with bone marrow infiltration and STAT mutations as supportive findings. T-LGLL generally has a favorable prognosis when treated with immunosuppressive agents like methotrexate or cyclophosphamide.
Natural Killer-cell Large Granular Lymphocytic Leukemia (NK-LGLL)
NK-LGLL shares many clinical features with T-LGLL, including cytopenias and autoimmune associations, but lacks TCR rearrangement. Morphologically indistinct from T-LGLL, diagnosis hinges on flow cytometric identification of aberrant NK-cell receptor expression (e.g., restricted KIR isoforms, altered CD94/NKG2A). STAT3 and TET2 mutations are common, with unique subtypes defined by CCL22 mutations. Though indolent, treatment is only initiated in symptomatic cases.
T-Prolymphocytic Leukemia (T-PLL)
T-PLL is a highly aggressive peripheral T-cell leukemia. It typically presents with marked lymphocytosis, splenomegaly, and lymphadenopathy. T-PLL is molecularly defined by TCL1A or MTCP1 rearrangements, often accompanied by ATM mutations and JAK/STAT pathway activation. Immunophenotyping reveals CD4+/CD8+ coexpression and overexpression of TCL1A, which helps differentiate it from LGLLs. Despite recent therapeutic advances such as alemtuzumab and stem cell transplant, prognosis remains poor.
Adult T-cell Leukemia/Lymphoma (ATLL)
ATLL is etiologically linked to HTLV-1 infection and typically affects individuals from endemic regions. Clinical presentation varies across four subtypes: acute, lymphomatous, chronic, and smoldering. Hallmark features include hypercalcemia, lymphadenopathy, and flower-like nuclei in atypical cells. Immunophenotyping shows CD4+/CD25+ expression with HTLV-1 integration confirmed via molecular techniques. Diagnosis requires demonstration of HTLV-1 proviral integration. Prognosis is subtype-dependent but generally guarded.
Sézary Syndrome (SS)
SS is a leukemic form of cutaneous T-cell lymphoma, presenting with erythroderma, lymphadenopathy, and circulating cerebriform T cells. Immunophenotypic markers include CD4 positivity with loss of pan-T-cell antigens and high PD1 expression. Genetic studies reveal clonal TCR rearrangement and frequent mutations in genes like STAT5B, TP53, and PLCG1. SS differs from LGLLs in morphology, skin tropism, and aggressive clinical course, with median survival around 32 months.
Aggressive NK-cell Leukemia (ANKL)
Though morphologically similar to LGLLs, ANKL is rapidly progressive, often associated with Epstein-Barr virus (EBV), and displays severe cytopenias and systemic symptoms. It is negative for TCR rearrangement and has a poor prognosis, necessitating prompt differentiation from indolent NK-LGLL.
Conclusion
This review highlights the diagnostic complexity of LGLLs and their mimics, emphasizing the importance of integrating morphological, immunophenotypic, and molecular data in line with the WHO 5th edition. Molecular mutations such as those in STAT3, TET2, and TCL1A play pivotal roles in refining classifications and prognostic stratification. While diagnostic clarity has improved, further large-scale studies are needed to validate these frameworks and explore novel therapeutic approaches tailored to individual molecular profiles.
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The study was recently published in the Journal of Clinical and Translational Pathology .
Journal of Clinical and Translational Pathology (JCTP) is the official scientific journal of the Chinese American Pathologists Association (CAPA). It publishes high quality peer-reviewed original research, reviews, perspectives, commentaries, and letters that are pertinent to clinical and translational pathology, including but not limited to anatomic pathology and clinical pathology. Basic scientific research on pathogenesis of diseases as well as application of pathology-related diagnostic techniques or methodologies also fit the scope of the JCTP.
