Clonal monosomy 7 and 5q--in a child with myelodysplastic syndrome

Pediatr Hematol Oncol. 2000 Sep;17(6):505-9. doi: 10.1080/08880010050120872.

Abstract

The authors report the case of a 5-year-old boy referred for thrombocytopenia and neutropenia. Bone marrow examination showed a myelodysplasia with clonal monosomy 7. The acceleration of the disease was marked by the appearance of an additional cytogenetic abnormality, i.e., the deletion of the long arm of chromosome 5 in the clonal cells. RAS gene mutation was not detected. Chemotherapy was started to achieve complete remission before a bone marrow transplantation. This treatment was complicated by a prolonged aplasia and the patient died of systemic mycotic infection.

Publication types

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

MeSH terms

  • Child, Preschool
  • Chromosome Deletion
  • Chromosomes, Human, Pair 5*
  • Chromosomes, Human, Pair 7*
  • Humans
  • Male
  • Monosomy*
  • Myelodysplastic Syndromes / genetics*