A 4-year-old child presents with pallor, fatigue, generalized petechiae, fever, and diffuse bone pain. Complete blood count shows hemoglobin 7.1 g/dL, white blood cell count 68,000/mm3, and platelets 22,000/mm3. Peripheral blood smear and bone marrow aspiration demonstrate 85% lymphoblasts expressing CD19, CD10, and TdT, without cytoplasmic immunoglobulins. Which cytogenetic abnormality in B-cell acute lymphoblastic leukemia (B-ALL) confers an unfavorable prognosis requiring treatment intensification?
- At(9;22)(q34;q11.2) [BCR-ABL1 / Philadelphia chromosome]
- BHyperdiploidy (> 50 chromosomes)
- Ct(12;21)(p13;q22) [ETV6-RUNX1]
- DTrisomy of chromosomes 4, 10, and 17