Chromosomal aberrations in Nigerians with haematological malignancies: preliminary report

Afr J Med Med Sci. 1993 Sep;22(3):21-7.

Abstract

Cytogenetic studies were carried out on the blood/bone marrow samples of three patients with chronic granulocytic leukaemia (CGL) and one patient with Burkitt's lymphoma. The karyotypes determined were 46, XY, Ph+ for patient O. A; 46, XY, t(9q+, 22q) for T. A. and 46, XX, t(9q+, 22q) for patient E. O. Patient O. L. with Burkitt's lymphoma presented two karyotypes: 46, XY and 46, XY, +18. The results showed that Philadelphia (Ph1) chromosome was detected in all the patients with CGL and a chromosome marker for African Burkitt's lymphoma in the boy with the disease.

Publication types

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

MeSH terms

  • Adult
  • Bone Marrow Examination
  • Burkitt Lymphoma / blood
  • Burkitt Lymphoma / diagnosis
  • Burkitt Lymphoma / genetics*
  • Child
  • Chromosome Aberrations / genetics*
  • Female
  • Genetic Markers
  • Humans
  • Karyotyping
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / blood
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / diagnosis
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
  • Male
  • Middle Aged
  • Nigeria
  • Philadelphia Chromosome

Substances

  • Genetic Markers