Acute T-lymphoblastic leukemia relapsed with the character of myeloid/natural killer cell precursor phenotype: a case

Shigeo Hashimoto1, Ken Toba, Sadao Aoki

  • 1First Department of Internal Medicine, Niigata University School of Medicine, Asahimachi-dori 1, Niigata City 951-8510, Japan.

Leukemia Research
|January 5, 2002
PubMed

Insights

This study tracks changes in acute lymphoblastic leukemia (ALL) cell markers during relapse. The findings suggest a potential link between ALL, myeloid/natural killer cell precursor acute leukemia, and immature T lymphoid precursors.

Area of Science:

  • Hematology
  • Oncology
  • Immunology

Background:

  • Acute lymphoblastic leukemia (ALL) is a heterogeneous lymphoid malignancy.
  • Understanding cell surface marker dynamics is crucial for accurate diagnosis and treatment.
  • The case presented initial ALL markers including CD7, CD13, CD33, CD34, HLA-DR, and cytoplasmic CD3ε.

Observation:

  • The patient was diagnosed with ALL and initially responded to chemotherapy.
  • The leukemia relapsed three times, showing significant alterations in cell phenotype.
  • Key changes included increased CD56 expression and decreased CD13, CD7, and cytoplasmic CD3ε.

Findings:

  • The relapsed leukemia phenotype shifted towards myeloid/natural killer cell precursor acute leukemia (M/NK-AL).
  • This phenotypic shift suggests a potential developmental relationship between ALL and M/NK-AL.
  • The observed changes indicate a possible evolution from immature T lymphoid precursors.

Implications:

  • This case highlights the importance of re-evaluating immunophenotypes in relapsed acute leukemias.
  • The findings may refine classifications of acute leukemias with myeloid and lymphoid features.
  • Further research into the relationship between ALL, M/NK-AL, and T-lymphoid precursors is warranted.