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The Biology of Chronic Graft-Versus-Host Disease

  • H. J. Deeg
Part of the Experimental Hematology book series (HEMATOLOGY)

Abstract

Chronic graft-versus-host (GVHD) disease occurs in as many as 30–50% of long-term survivors after allogeneic marrow transplantation, even when the donor was an HLA genotypically identical sibling (1, 2). Because of severe morbidity and mortality associated with this syndrome, it has a major effect on long-term results of clinical marrow transplantation (3). Chronic GVHD generally develops within 3 months to one year after transplantation. Three forms of onset have been recognized (4): 1) Progressive chronic GVHD, i.e. as a continuation of acute GVHD, 2) quiescent chronic GVHD, i.e. after a disease-free, asymptomatic interval following acute GVHD, and 3) de novo chronic GVHD in patients who never had any clinical manifestation of acute GVHD. The prognosis is the worst for patients with progressive chronic GVHD, intermediate with quiescent, and best with de novo chronic GVHD.

Keywords

Aplastic Anemia Acute GVHD Chronic GVHD Autoimmune Hemolytic Anemia Marrow Graft 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 1985

Authors and Affiliations

  • H. J. Deeg
    • 1
  1. 1.Fred Hutchinson Cancer Research Center and the University of Washington School of MedicineSeattleUSA

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