Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia

Cancer Genet Cytogenet. 2006 Aug;169(1):58-61. doi: 10.1016/j.cancergencyto.2006.02.007.

Abstract

We describe the rare finding of a 33-month-old child neonatally diagnosed with Down syndrome, who presented with pre-B acute lymphoblastic leukemia (ALL) with a pretreatment bone marrow karyotype in which a low hypodiploid cell line (38 chromosomes) was identified in 17/19 cells studied. The abnormal cell line retained the extra constitutional chromosome 21. Hypodiploidy (loss of one or more chromosomes) is seen in approximately 5% of all childhood pre-B ALL cases and in approximately 2.2% cases of individuals with a constitutional trisomy 21. Low hypodiploidy, associated with a high risk of relapse, is rare in pediatric ALL cases in the general population, and, to our knowledge, is previously unreported in patients with trisomy 21.

Publication types

  • Case Reports

MeSH terms

  • Burkitt Lymphoma / complications
  • Burkitt Lymphoma / genetics*
  • Child, Preschool
  • Diploidy*
  • Down Syndrome / complications
  • Down Syndrome / genetics*
  • Female
  • Humans
  • Karyotyping
  • Male