Abstract
Due to its rare incidence, erythrocytosis frequently represents a challenge for the
treating doctors. The erythropoiesis (= production of erythrocytes) is located in
the bone marrow, and the hormone erythropoietin (EPO) takes control in its regulation.
Therefore, measurement of EPO in serum is one of the main diagnostic steps. In erythrocytosis,
congenital causes have to be distinguished from acquired ones. Furthermore, there
are primary and secondary forms. Congenital causes of erythrocytoses occur very infrequently,
are mainly diagnosed in young age and should be treated in specialized centers. Polycythemia
vera (PV), a clonal disorder and one of the main myeloproliferative neoplasms (beside
essential thrombocythemia and primary myelofibrosis), represents the most frequent
primary acquired cause of erythrocytosis. Clinically, increased thrombophilia and
microvascular disturbance occur. The first-line treatment in patients with PV includes
administration of aspirin and phlebotomies. Secondary acquired forms of erythrocytosis
mainly occur due to hypoxia triggered by nicotine abuse or chronic heart and lung
diseases. Regarding other differential diagnoses, a cancer-associated EPO production,
kidney diseases or exogenous supply with EPO (= EPO doping) have to be considered.
Pathologische Veränderungen der absoluten Erythrozytenzahl finden in Routinelaboruntersuchungen
meist wenig Beachtung. Im Gegensatz zu den Erythrozytopenien als Ausdruck einer Anämie
kommt es im Falle einer Erythrozytose bezüglich des weiteren Vorgehens häufig zu Unsicherheiten.
Lesen Sie im folgenden Artikel, welche Ursachen bei einer Erythrozytose vorliegen
können und welche diagnostischen und therapeutischen Schritte einzuleiten sind.
Schlüsselwörter
Erythrozytose - EPO - Polycythaemia vera - Gewebshypoxie - Doping
Key words
erythrocytosis - polycythemia vera - hypoxia - doping