Ultrastructural and chromosomal studies in a patient with hypergranular (M3) promyelocytic leukemia with two abnormal clones

I. Zahavi, F. Shabtai, S. Appel, C. Rudniki, M. Djaldetti

Research output: Contribution to journalArticlepeer-review

Abstract

The internal and surface ultrastructural features of the white blood cells of a patient with hypergranular (M3) promyelocytic leukemia are described. Cytogenetical studies of the patient’s cells revealed the presence of two abnormal clones: The first, 45, XY, -7, and the second with an interstitial deletion in the long arm of chromosome 15 with break points at q22 and q26.

Original languageEnglish
Pages (from-to)52-57
Number of pages6
JournalActa Haematologica
Volume68
Issue number1
DOIs
StatePublished - 1982

Keywords

  • Cell ultrastructure
  • Chromosomal translocation
  • Electron microscopy
  • Hypergranular (M) promyelocytic leukemia

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