T-Cell Large Granular Lymphocytic Leukemia with Extremely Rare Immunophenotype (CD4/CD8 Double-Positive) Followed by

Dina Soliman1,2,3, Sherin Sallam2, Susanna Akiki1,2

  • 1Department of Laboratory Medicine and Pathology, National Center for Cancer Care and Research, Hamad Medical Corporation, Doha, Qatar.

Insights

This study reports the first case of asymptomatic CD4/CD8 double-positive T-cell large granular lymphocytic leukemia (T-LGLL). The rare T-LGLL phenotype was diagnosed and later associated with multiple myeloma.

Area of Science:

  • Hematology
  • Immunology
  • Oncology

Background:

  • T-cell large granular lymphocytic leukemia (T-LGLL) involves clonal expansion of CD3+/CD57+ cytotoxic T-cells.
  • Diagnosis requires persistent LGL elevation (>6 months) without an identifiable cause.
  • T-LGLL is linked to autoimmune diseases, infections, and malignancies.

Observation:

  • A case of asymptomatic CD4/CD8 double-positive T-LGLL is presented.
  • Flow cytometry identified a T-LGLL subpopulation expressing CD57 and cTIA.
  • T-cell receptor repertoire analysis and PCR confirmed clonality.

Findings:

  • The patient was diagnosed with IgG kappa multiple myeloma six months after the T-LGLL diagnosis.
  • This represents the first reported case of CD4/CD8 double-positive T-LGLL.
  • The rarity suggests underreporting or a genuinely rare clinical entity.

Implications:

  • Further research is needed to understand the pathogenesis and clinical features of this T-LGLL phenotype.
  • The relationship between T-LGLL and multiple myeloma warrants investigation.
  • This case highlights the importance of recognizing rare T-LGLL variants.