Author/Authors :
Vendrame-Goloni، نويسنده , , Cristina Benitez and Varella-Garcia، نويسنده , , Marileila and Carvalho-Salles، نويسنده , , Andréa Borduchi and Ruiz، نويسنده , , Milton Artur and Jْnior، نويسنده , , Otلvio Ricci and Fett-Conte، نويسنده , , Agnes Cristina، نويسنده ,
Abstract :
A novel association of t(11;19)(q23;p13) and t(5;16)(q13;q22) was detected by G-banding and spectral karyotyping studies in an 18-year-old patient. While balanced t(11;19) has been often described in acute myelocytic leukemia (AML) French–American–British Cooperative Group subtypes M4 and M5, this patient was diagnosed with the variant AML-M4 with eosinophilia (AML-M4Eo), which is associated with abnormalities in 16q22 and has good prognosis. However, the patient relapsed after allogeneic transplant and died within 2 years of diagnosis, which suggests that the association of these two translocations correlates with a poor prognosis. This report expands the molecular basis of the variability in clinical outcomes and adds the novel t(5;16)(q13;q22) to the spectrum of chromosome 16q22 abnormalities in AML.