Molecular biology of polycythemias

Authors
Citation
Jt. Prchal, Molecular biology of polycythemias, INTERN MED, 40(8), 2001, pp. 681-687
Citations number
103
Categorie Soggetti
General & Internal Medicine
Journal title
INTERNAL MEDICINE
ISSN journal
09182918 → ACNP
Volume
40
Issue
8
Year of publication
2001
Pages
681 - 687
Database
ISI
SICI code
0918-2918(200108)40:8<681:MBOP>2.0.ZU;2-C
Abstract
Polycythemia is literally translated as "many cells in the blood". Only ery throcytosis (an alternative term for these disorders) produces polycythemia since leukocytes and platelets are present in blood in far smaller proport ions. Polycythemia may be due to increased proliferation or decreased apopt osis of erythroid progenitors, or to delayed erythroid differentiation with an increased number of progenitor cell divisions. Prolonged red cell survi val, another theoretical cause of polycythemia, has not yet been described and with intact regulatory mechanisms is unlikely to occur. Primary polycyt hemias result from abnormalities expressed in hematopoietic progenitors. In contrast, circulating factors cause secondary polycythemia (1). There are acquired and congenital causes of both primary and secondary polycythemia ( 1).