Chronic myeloid leukaemia is characterised by a single genetic translocation (bcr-abl) in a pluripotent stem cell. It is characterised by increased proliferation of differentiating granulocytic cells. The peripheral blood shows an increased number of granulocytes and occasional blasts. 90-95% of cases present with the Philadelphia chromosome – a shorter chromosome 22 formed by a reciprocal translocation between 9q and 22q; t9;22.
CML accounts for 20% of cases of leukaemia. It peaks at 60 – 70 years of age.
Stages of CML
Stage
Description
Chronic phase
Stable and asymptomatic with < 10% of blasts in blood and bone marrow aspirate. Infection and bleeding complications are rare.
Accelerated phase
10-19% blasts in the blood and bone marrow aspirate. CBC shows Basophilia (>20%) and Thrombocytopenia
Blast crisis
> 20% blasts in the blood and blood. Resembles AML. It is generally fatal.
Risk factors for CML
Ionizing radiation
Chemicals e.g benzene
Pathogenesis
The ABL oncogene encodes a tyrosine-protein kinase
The ABL oncogene is relocated from 9q to a specific breakpoint cluster region (BCR) in 22q.
The fusion oncogene BCR-ABL1 encodes a strong tyrosine kinase in hematopoietic progenitor cells
The tyrosine kinase is constitutively activated and confers proliferative and anti-apoptotic effects
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