An unusual case of chronic lymphocytic leukemia with trisomy 12 presenting with prolymphocytic transformation and t(8;21)(q22;q22)

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.

Detalles Bibliográficos
Autores principales: Bhushan, Mishi, Kumar, Kirthi R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Clinical Images
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077250/
https://www.ncbi.nlm.nih.gov/pubmed/33936733
http://dx.doi.org/10.1002/ccr3.4059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077250/
https://www.ncbi.nlm.nih.gov/pubmed/33936733
http://dx.doi.org/10.1002/ccr3.4059

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