Conceptual
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Pathophysiology of Chronic Myeloid and Chronic Lymphocytic Leukemia in Hematology

Chronic leukemias arise when an acquired chromosomal abnormality (deletion, trisomy, or translocation) in a hematopoietic stem cell destined for the leukocyte lineage disrupts normal maturation and cell-cycle control, producing large numbers of partially matured leukocytes that accumulate and crowd out healthy hematopoiesis. Chronic myeloid leukemia (CML) results from a specific reciprocal translocation forming the Philadelphia chromosome and its constitutively active BCR-ABL tyrosine kinase, driving excessive granulocyte division, while chronic lymphocytic leukemia (CLL) results from varied chromosomal mutations disrupting B-cell receptor signaling pathways, causing B lymphocytes to fail to die on schedule; both fall within hematologic oncology and are distinguished from acute leukemias by partial (rather than absent) cell maturation.