Chediak-Higashi syndrome

Am J Pediatr Hematol Oncol. 1987 Spring;9(1):42-55. doi: 10.1097/00043426-198721000-00008.


The use of cytochemical, electron microscopic, immunofluorescent, and tissue culture techniques has led to important advances in our understanding of the mechanisms underlying the pathogenesis of the Chediak-Higashi syndrome (CHS). This rare and fatal autosomal recessive disorder is clinically characterized by partial albinism, frequent pyogenic infections, and an accelerated lymphohistiocytic phase. The pathological hallmark of CHS is the presence in all white blood cells of massive lysosomal inclusions, which are formed through a combined process of fusion, cytoplasmic injury, and phagocytosis. The abnormal inclusions exhibit both azurophilic and specific granular markers, and are probably responsible for most of the impaired leukocyte and other cell functions in CHS patients. In addition, a selective profound natural killer (NK) cell function and platelet storage pool deficiencies have been described in these patients. Impaired microtubule assembly and functions, mediated by abnormal intracellular cyclic nucleotide levels, which could be corrected by treatment with ascorbic acid, were suggested to be the pathophysiological basis for CHS abnormalities. However, some recent studies have questioned this cytoskeletal model, which is suggested to be rather a secondary manifestation of CHS.

Publication types

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

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Ascorbic Acid / therapeutic use
  • Bacterial Infections / etiology
  • Bone Marrow / ultrastructure
  • Chediak-Higashi Syndrome / blood
  • Chediak-Higashi Syndrome / complications
  • Chediak-Higashi Syndrome / genetics
  • Chediak-Higashi Syndrome / physiopathology*
  • Cytoplasmic Granules / metabolism
  • Cytoplasmic Granules / ultrastructure
  • Histocytochemistry
  • Humans
  • Killer Cells, Natural / physiology
  • Leukocytes / cytology
  • Leukocytes / enzymology
  • Microscopy, Electron
  • Microtubules / physiology
  • Microtubules / ultrastructure


  • Antineoplastic Agents
  • Ascorbic Acid