Abstract
The aplastic anemias are characterized by peripheral blood pancytopenia, bone marrow hypocellularity, and absence of a clonal hematological process. They have an incidence of approximately two patients per million population in the West and four per million in Asia.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Suggested Reading
Hall C, Richards S, Hillman P. Primary prophylaxis with warfarin prevents thrombosis in paroxysmal nocturnal hemoglobinuria (PNH). Blood 2003;102:3587–3591.
Marsh JC, Ball SE, Darbyshire P, et al; British Committee for Standards in Haematology Guidelines for the diagnosis and management of acquired aplastic anaemia Br J Haematol 2003;123:782–801
Young NS, Maciejewski J. The pathophysiology of aplastic anemia N Engl J Med 1997;336:1365–1372
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2007 Humana Press Inc., Totowa, NJ
About this chapter
Cite this chapter
Paquette, R., Munker, R. (2007). Aplastic Anemias. In: Munker, R., Hiller, E., Glass, J., Paquette, R. (eds) Modern Hematology. Contemporary Hematology. Humana Press. https://doi.org/10.1007/978-1-59745-149-9_12
Download citation
DOI: https://doi.org/10.1007/978-1-59745-149-9_12
Publisher Name: Humana Press
Print ISBN: 978-1-58829-557-6
Online ISBN: 978-1-59745-149-9
eBook Packages: MedicineMedicine (R0)