Karyotype evolution in a patient with biphenotypic neonatal leukemia

Cancer Genet Cytogenet. 1992 Sep;62(2):124-9. doi: 10.1016/0165-4608(92)90249-8.

Abstract

We present the case of a 4-day-old boy with acute lymphoblastic leukemia showing at onset a karyotype 46,XY,t(4;11)(q21;q23). At relapse an additional change, add(2), was present. Molecular analysis showed the same immunoglobulin rearrangement both at onset and at relapse, but immunohistochemical analysis revealed some cells having myeloid features. A continuous cell line derived from the leukemic blasts of the patient presented typical monoblastic features.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 4
  • Gene Rearrangement
  • Humans
  • Immunophenotyping
  • Infant, Newborn
  • Karyotyping
  • Leukemia, Lymphoid / congenital*
  • Leukemia, Lymphoid / genetics
  • Leukemia, Myeloid / congenital*
  • Leukemia, Myeloid / genetics
  • Male
  • Translocation, Genetic