Hypoplastic myelodysplastic syndrome-a clinical, morphologic, or genetic diagnosis?

Cancer Genet Cytogenet. 2002 Oct 1;138(1):85-8. doi: 10.1016/s0165-4608(02)00581-2.

Abstract

We report a middle-aged female with an 11-year history of nonprogressive pancytopenia and severely hypoplastic marrow with minimal morphologic dysplasia. A diagnosis of hypoplastic myelodysplastic syndrome (MDS) was made because of the finding of a persistent clonal abnormality, del(13)(q12q14), and the subsequent demonstration of a single Auer rod-containing blast in the peripheral blood smear. The case illustrates the problems in the differentiation between aplastic anemia and hypoplastic MDS.

Publication types

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

MeSH terms

  • Adult
  • Bone Marrow / pathology
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 13 / genetics*
  • Female
  • Humans
  • Karyotyping
  • Megakaryocytes / pathology
  • Myelodysplastic Syndromes / diagnosis*
  • Myelodysplastic Syndromes / genetics*
  • Myelodysplastic Syndromes / pathology