Pathogenesis of hypofibrinogenemia in familial hemophagocytic lymphohistiocytosis

Pediatr Pathol. 1991 Jul-Aug;11(4):657-61. doi: 10.3109/15513819109064797.

Abstract

In order to investigate the cause of hypofibrinogenemia in familial hemophagocytic lymphohistiocytosis (FHL), formalin-fixed and paraffin-embedded tissue sections of the spleen obtained at autopsy were examined by using immunohistochemical methods for the presence of fibrinogen antigens, and such antigens were detected in approximately 10% of the histiocytes in a diffuse staining pattern. This finding indicates uptake of fibrin and/or fibrinogen molecules by activated histiocytes and suggests that hypofibrinogenemia of FHL is caused by the direct action of activated histiocytes on factor X through Mac-1 receptors, subsequent activation of the common pathway of the coagulation protease cascade, and uptake of fibrin and/or fibrinogen molecules by such cells.

MeSH terms

  • Afibrinogenemia / etiology*
  • Afibrinogenemia / genetics
  • Afibrinogenemia / pathology
  • Factor X / metabolism
  • Histiocytes / metabolism
  • Histiocytes / pathology
  • Histiocytosis, Non-Langerhans-Cell / blood*
  • Histiocytosis, Non-Langerhans-Cell / genetics
  • Histiocytosis, Non-Langerhans-Cell / pathology
  • Humans
  • Infant
  • Macrophage-1 Antigen / metabolism
  • Spleen / metabolism
  • Spleen / pathology

Substances

  • Macrophage-1 Antigen
  • Factor X