Onkologie. 2015:9(1):38-42
Childhood acute lymphoblastic leukemia, like cancer in general, probably arises from interactions between exogenous or endogenous
exposures, genetic susceptibility, and chance. This multistep process begins sometimes even during prenatal period of life. Abnormal
response to a common infection remains the strongest candidate for causal exposure. More precise risk stratification and personalized
chemotherapy based on the biological characteristics of leukemic cells and hosts (prognostic and/or predictive genetic markers, minimal
residual disease monitoring) have pushed the cure rate of childhood acute lymphoblastic leukemia to near 90 %. However with the exception
of infant leukemia, which still bears a dismal prognosis. Many new genetic techniques are approaching to clinical praxis mostly
based on microarray or next-generation sequencing techniques. The strong point of well-established cytogenetic analysis remains in
the possibility of a complex view to the whole karyotype of pathological cells. This kind of view allows us to understand the origin of
genetic abnormalities and diversity of cancer cells in the form of evolving new subclones. The main goal of the presented case reports
is to bring attention to this specific advantage of cytogenetic analysis.
Published: March 10, 2015 Show citation