Macrophage activation syndrome

Curr Opin Rheumatol. 2002 Sep;14(5):548-52. doi: 10.1097/00002281-200209000-00012.

Abstract

Macrophage activation syndrome (MAS) is a serious complication of childhood systemic inflammatory disorders that is thought to be caused by excessive activation and proliferation of T lymphocytes and macrophages. Recent findings in hemophagocytic lymphohistiocytosis, a disease that is clinically similar to MAS, highlight the possible pathogenetic role of a defective function of perforin, a protein involved in the cytolytic processes and control of lymphocyte proliferation. Although the clinical features of MAS have been well documented, early diagnosis can be difficult. Measurement of the serum ferritin level may assist in the diagnosis and may be a useful indicator of disease activity, therapy response, and prognosis. The recognition that MAS belongs to the secondary or reactive hemophagocytic syndromes has led to the proposal to rename it according to the contemporary classification of histiocytic disorders. Cyclosporin A has been found effective in patients with corticosteroid-resistant MAS. A recent report has suggested that etanercept may be a useful adjunctive therapeutic agent.

Publication types

  • Review

MeSH terms

  • Arthritis, Juvenile / complications
  • Arthritis, Juvenile / pathology*
  • Arthritis, Juvenile / therapy
  • Child
  • Cyclosporine / therapeutic use
  • Etanercept
  • Ferritins / blood
  • Glucocorticoids / therapeutic use
  • Histiocytosis, Non-Langerhans-Cell / pathology
  • Humans
  • Immune System Diseases / etiology
  • Immune System Diseases / pathology*
  • Immune System Diseases / therapy
  • Immunoglobulin G / therapeutic use
  • Macrophage Activation*
  • Receptors, Tumor Necrosis Factor / therapeutic use
  • Syndrome

Substances

  • Glucocorticoids
  • Immunoglobulin G
  • Receptors, Tumor Necrosis Factor
  • Cyclosporine
  • Ferritins
  • Etanercept