An unusual case of chronic lymphocytic leukemia with trisomy 12 presenting with prolymphocytic transformation and t(8;21)(q22;q22)
Abstract First report of t(8;21)(q22;q22) in a patient with CLL. RUNX1‐RUNX1T1 fusion gene resulting from the translocation may have played a role in the prolymphocytic transformation.
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2021-04-01
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Series: | Clinical Case Reports |
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Online Access: | https://doi.org/10.1002/ccr3.4059 |