Idiopathic thrombocytopenic purpura: a case of particular historic interest

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Abstract

Idiopathic thrombocytopenic purpura (ITP) is a disease in which the blood platelets are affected by autoantibodies and are removed from the bloodstream by the spleen and other reticuloendothelial tissue. The resulting bleeding disorder may be a transient sequel to childhood viral infections, but in other circumstances it is a prolonged and serious disease of children and adults. A case is reported of the first successful treatment of chronic ITP in England. It highlights the characteristics of the disease and an unusual complication.

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Bannister, B. A., Wonke, B., & Clendinnen, B. G. (1980). Idiopathic thrombocytopenic purpura: a case of particular historic interest. Journal of the Royal Society of Medicine, 73(11), 828–829. https://doi.org/10.1177/014107688007301113

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