Historical perspective and clinical implications of the Pelger-Hüet cell

Am J Hematol. 2009 Feb;84(2):116-9. doi: 10.1002/ajh.21320.

Abstract

The unique historical aspects of Pelger and Huet's discovery of the Pelger-Huet cell highlight the diagnostic challenge that this morphologic finding presents to the physician. Making the diagnosis of the benign autosomal dominant anomaly is complicated by the morphologically similar pseudo-Pelger-Huet cell, which can signify underlying myeloid dsyplasia. This article relates the history of the Pelger-Huet anomaly as well as describes the clinical significance and diagnostic workup for the finding of a Pelger-Huet cell on peripheral smear.

Publication types

  • Historical Article

MeSH terms

  • Animals
  • Cell Nucleus / ultrastructure
  • Child
  • Diagnosis, Differential
  • Eosinophils / pathology
  • Female
  • Fetal Death / genetics
  • Genes, Dominant
  • History, 20th Century
  • Humans
  • Infections / blood
  • Lamin B Receptor
  • Leukemia, Myeloid / blood
  • Leukemia, Myeloid / diagnosis
  • Myelodysplastic Syndromes / blood
  • Myelodysplastic Syndromes / diagnosis
  • Netherlands
  • Neutrophils / pathology*
  • Pedigree
  • Pelger-Huet Anomaly* / blood
  • Pelger-Huet Anomaly* / diagnosis
  • Pelger-Huet Anomaly* / genetics
  • Pelger-Huet Anomaly* / history
  • Receptors, Cytoplasmic and Nuclear / deficiency
  • Receptors, Cytoplasmic and Nuclear / genetics

Substances

  • Receptors, Cytoplasmic and Nuclear