Myelodysplastic syndrome with partial deletion of the long arm of chromosome 5: first report of a case in a child

Acta Paediatr Jpn. 1992 Oct;34(5):539-42. doi: 10.1111/j.1442-200x.1992.tb01003.x.

Abstract

A childhood case of myelodysplastic syndrome (MDS) with a deletion of the long arm of chromosome 5 (5q-) is reported. The patient was an 8 year old boy who has recurrent angina. Laboratory evaluation revealed the following: hemoglobin 8.1 gm/dl, white blood cell count 4.9 x 10(3)/l with 3% atypical lymphocytes, and platelet count 17.7 x 10(4)/l. A bone marrow aspirate revealed 20% blast cells and dysmyelopoietic changes involving all three marrow cell lines. Karyotype analysis of marrow cells revealed 46,XY,5q- in 100% of the metaphases. These findings led to a diagnosis of MDS with 5q-, which is most commonly found in adult MDS. This case seems to represent an exceedingly rare childhood case of MDS with 5q-.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Bone Marrow Examination
  • Child
  • Chromosome Aberrations / diagnosis
  • Chromosome Aberrations / genetics*
  • Chromosome Deletion*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 5*
  • Humans
  • Karyotyping
  • Male
  • Myelodysplastic Syndromes / complications*
  • Myelodysplastic Syndromes / diagnosis
  • Pharyngitis / etiology
  • Recurrence