Korean J Pediatr.  2007 Jun;50(6):519-523. 10.3345/kjp.2007.50.6.519.

Aplastic anemia

Affiliations
  • 1Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea. kimhk@catholic.ac.kr

Abstract

Aplastic anemia is a rare disease, which is characterized by pancytopenia and hypocellular bone marrow without infiltration of abnormal cells or fibrosis. The incidence in Asia is higher than in the West and new cases are diagnosed at a rate of 5.1 per million pediatric populations per year in Korea. The pathophysiology is understood roughly by defective hematopoiesis, impaired bone marrow microenvironment and immune mechanism. Treatments are performed on basis of pathogenesis and selected depending on the severity. Immunosuppressive therapy with antilymphocyte or antithymocyte globulin and cyclosporine is effective in the majority of patients but has some problems including relapse or clonal evolution. Recently, there have been clinical trials of immunosuppression with hematopoietic growth factors or other drugs. Allogeneic hematopoietic stem cell transplantation (HSCT) is curative in children with severe aplastic anemia. The overall survival in HSCT from HLA-identical sibling is higher than alternative donor, including HLA matched unrelated donor or cord blood. We have to consider quality of life after HSCT because of high survival rate. However, chronic graft versus host disease and graft failure are important factors that affect the quality of life and overall survival. We need further investigation to make new regimens aimed at overcoming these risk factors and perform clinical trials.

Keyword

Aplastic anemia; Immunosuppressive therapy; Allogeneic hematopoietic stem cell transplantation

MeSH Terms

Anemia, Aplastic*
Antilymphocyte Serum
Asia
Bone Marrow
Child
Clonal Evolution
Cyclosporine
Fetal Blood
Fibrosis
Graft vs Host Disease
Hematopoiesis
Hematopoietic Stem Cell Transplantation
Humans
Immunosuppression
Incidence
Intercellular Signaling Peptides and Proteins
Korea
Pancytopenia
Quality of Life
Rare Diseases
Recurrence
Risk Factors
Siblings
Survival Rate
Tissue Donors
Transplants
Unrelated Donors
Antilymphocyte Serum
Cyclosporine
Intercellular Signaling Peptides and Proteins
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