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Published on: March 30, 2018
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.
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.
Abstract:
The leukemic lymphoblasts of a patient expressed CD7, CD13, CD33, CD34, HLA-DR and cytoplasmic CD3varepsilon. He was diagnosed with acute lymphoblastic leukemia (ALL), and successfully treated with a conventional chemotherapy for ALL. The disease relapsed three times, and the character of the cells gradually altered, i.e. CD56 expression increased and CD13, CD7 and cCD3 epsilon decreased. The phenotype of the relapsed ALL was, therefore, compatible with myeloid/natural killer cell precursor acute leukemia (M/NK-AL). Some of M/NK-AL may be closely related with T/myeloid-biphenotypic pro-T blasts, and both types of acute leukemia may develop a tendency to express myeloid antigens, and they may belong to the category of immature T lymphoid precursors.
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