Management of immune thrombocytopenic purpura in adults.

@article{Stasi2004ManagementOI,
  title={Management of immune thrombocytopenic purpura in adults.},
  author={Roberto Stasi and Drew dkk Provan},
  journal={Mayo Clinic proceedings},
  year={2004},
  volume={79 4},
  pages={
          504-22
        }
}
Primary immune thrombocytopenic purpura (ITP), also referred to as idiopathic thrombocytopenic purpura, is an organ-specific autoimmune disorder in which antibody-coated or immune complex-coated platelets are destroyed prematurely by the reticuloendothelial system, resulting in peripheral blood thrombocytopenia. The disease is heterogeneous with regard to its severity and clinical course and is unpredictable in its response to therapy. Although the basic underlying pathophysiology of ITP has… CONTINUE READING
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