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Acta Medica Medianae
Vol. 47, No3 , October, 2008
UDK 61
YU ISSN 0365-4478


Correspondence to:

Irena Ćojbašić

Klinika za hematologiju i kliničku imunologiju

Bulevar Zorana Đinđića 48,

18000 Niš, Srbija

E-mail: icojbasic@gmail.com











Copyright 2008 by Faculty  of Medicine, University of Nis

Professional article




Irena Cojbasic and Lana Macukanovic-Golubovic



Essential thrombocytosis (ET) is clonal chronic myeloprolifertive disorder which originates from abnormality of a multipotent hematopoietic stem cell.

It is characterized by an increased platelet count, megakaryocytic hyperplasia and by hemorrhagic or thrombotic tendency. Symptoms and signs may include weakness, headaches, paresthesias, bleeding, splenomegaly, and digital ischemia. ET patients showed equal or slightly shorter survival than age- and sex-matched healthy population. Major causes of death were  thrombotic and hemorrhagic complications or malignant progression due to both the natural history of the disease and, possibly, the use of chemotherapeutic agents.

Diagnostic criteria for essential thrombocythemia were proposed in 2005 by the PVSG and demand diagnosis of exclusion.

Myelosuppressive therapy to lower the platelet count usually consists of hydroxyurea, interferon alfa or anagrelide. Hydroxyurea is the most commonly used treatment, because of its efficacy, low cost and rare acute toxicity. Interferon alfa is a biological response modifier. It is not known to be teratogenic and does not cross the placenta, and is often the treatment of choice during pregnancy. Anagrelid suppresses bone marrow megakaryocytes by interfering with the maturation process and decreasing platelet production without affecting other blood cell lines. Low-dose aspirin may be used to control microvascular symptoms.

Recommendations for management of patients with essential thrombocythemia were given by ASH. From a treatment standpoint, hydroxyurea is now confirmed to be the drug of choice for high-risk patients with essential thrombocythemia. Interferon alfa and anagrelide are reasonable second-line agents. Low-risk patients should receive low-dose aspirin alone. For the intermediate-risk patients, a consensus could not be reached on a recommendation for platelet-lowering treatment. Acta Medica Medianae 2008;47(3):51-55.


Key words: essential thrombocythemia, recommendation, treatment

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