Abstract
The chronic myeloproliferative disorders are clonal diseases of the hematopoietic stem cell. Polycythemia vera (PV) is characterized by extensive trilineage bone marrow hyperplasia, whereas in essential thrombocythemia (ET), proliferation of the megakaryocytic lineage prevails. Both diseases run a relatively benign clinical course, and survival is almost normal. Morbidity and mortality result primarily from vascular complications, i.e., thromboembolism, micro circulatory disorders, and bleeding. Other symptoms include pruritus, splenomegaly, and in PV plethora, arterial hypertension, and signs of iron deficiency.
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Wehmeier, A. (1997). Interferon Therapy of Essential Thrombocythemia and Polycythemia Vera. In: Aul, C., Schneider, W. (eds) Interferons. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-60411-9_6
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