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Aplastic Anemias

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Modern Hematology

Part of the book series: Contemporary Hematology ((CH))

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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.

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Suggested Reading

  • Hall C, Richards S, Hillman P. Primary prophylaxis with warfarin prevents thrombosis in paroxysmal nocturnal hemoglobinuria (PNH). Blood 2003;102:3587–3591.

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  • 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

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  • Young NS, Maciejewski J. The pathophysiology of aplastic anemia N Engl J Med 1997;336:1365–1372

    CAS  Google Scholar 

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© 2007 Humana Press Inc., Totowa, NJ

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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

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  • 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)

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