Sequential observation of clinical and karyotypic evolution in a patient with myelodysplastic syndrome

Chin Med J (Engl). 1989 Sep;102(9):689-94.

Abstract

This paper reports an interesting case of myelodysplastic syndrome (MDS), whose bone marrow karyotype at diagnosis was 46, XY, t(16;17) (q12;q25). Fourteen months later, the disease transformed into erythroleukemia, and several correlative clones with hyperdiploid appeared at the same time. Thus, we consider that detecting karyotypic evolution may help evaluate the prognosis of MDS.

Publication types

  • Case Reports

MeSH terms

  • Anemia, Refractory / genetics
  • Anemia, Refractory / pathology
  • Bone Marrow / pathology
  • Chromosome Aberrations / genetics
  • Chromosome Disorders
  • Chromosomes, Human, Pair 16
  • Chromosomes, Human, Pair 17
  • Humans
  • Karyotyping*
  • Leukemia, Erythroblastic, Acute / pathology
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / genetics*
  • Myelodysplastic Syndromes / pathology
  • Prognosis