Aplastic anemia surgery: Difference between revisions
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{{Aplastic anemia}} | {{Aplastic anemia}} | ||
'''Editor-In-Chief:''' Aric Hall, M.D., Beth Israel Deaconess Medical Center, Boston, MA [mailto:achall@bidmc.harvard.edu] | '''Editor-In-Chief:''' Aric Hall, M.D., Beth Israel Deaconess Medical Center, Boston, MA [mailto:achall@bidmc.harvard.edu] |
Revision as of 18:08, 13 August 2015
Aplastic anemia Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Aplastic anemia surgery On the Web |
American Roentgen Ray Society Images of Aplastic anemia surgery |
Risk calculators and risk factors for Aplastic anemia surgery |
Editor-In-Chief: Aric Hall, M.D., Beth Israel Deaconess Medical Center, Boston, MA [1]
Overview
Surgery
Surgery and Device Based Therapy
Treating aplastic anemia involves suppression of the immune system, an effect achieved by daily medicine intake, or, in more severe cases, a bone marrow transplant, a potential cure but a risky procedure. The transplanted bone marrow replaces the failing bone marrow cells with new ones from a matching donor. The pluripotent stem cells in the bone marrow reconstitute all three blood cell lines, giving the patient a new immune system, red blood cells, and platelets. However, besides the risk of graft failure, there is also a risk that the newly created white blood cells may attack the rest of the body ("graft-versus-host disease").