Biclonal B-cell chronic lymphocytic leukemia with inv(14)(q11q32)

K F Wong1, C C So

  • 1Department of Pathology, Queen Elizabeth Hospital, Hong Kong.

Insights

Cytogenetic biclonality, the presence of two distinct cell populations, is rare in chronic lymphocytic leukemia. This case highlights a patient with B-cell chronic lymphocytic leukemia exhibiting two unrelated clones, one with an inv(14) abnormality.

Area of Science:

  • Hematology
  • Oncology
  • Cytogenetics

Background:

  • Chronic lymphocytic leukemia (CLL) is a mature B-cell neoplasm.
  • Cytogenetic abnormalities are common in CLL and impact prognosis.
  • Cytogenetic biclonality, defined by two distinct karyotypically aberrant cell populations, is infrequently reported in CLL.

Purpose of the Study:

  • To report a rare case of cytogenetic biclonality in B-cell chronic lymphocytic leukemia.
  • To describe the immunophenotypic and cytogenetic findings in a patient with dual clonal populations.

Main Methods:

  • Diagnosis of B-cell chronic lymphocytic leukemia based on morphology and immunophenotype (CD5+, CD19+, CD23+).
  • Karyotypic analysis of peripheral blood lymphocytes.
  • Identification of distinct cytogenetic clones.

Main Results:

  • The patient presented with typical B-cell chronic lymphocytic leukemia.
  • Karyotypic analysis revealed two distinct, unrelated cytogenetic clones in the leukemic cells.
  • One of the identified clones harbored an inversion of chromosome 14, specifically inv(14).

Conclusions:

  • Cytogenetic biclonality can occur in B-cell chronic lymphocytic leukemia, albeit rarely.
  • The presence of multiple clones may have implications for disease behavior and treatment.
  • Further investigation is warranted to understand the clinical significance of biclonality in CLL.

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