Name: | Description: | Size: | Format: | |
---|---|---|---|---|
52.19 KB | Adobe PDF |
Authors
Advisor(s)
Abstract(s)
Essential Thrombocythemia (ET) is a rare disease in
pediatric age. The dominant clinical manifestations are thrombotic
(arterial or venous) and/or hemorrhagic, but most of the cases
are asymptomatic, and diagnosis made by routine hemogram.
A previously healthy adolescent, federated football player,
was oriented to the paediatric haematology consultation, at the
age of 15 years, because of the presence of sustained thrombocytosis.
It was established the diagnosis of Essential Thrombocythemia
based on the criteria of the World Health Organization (WHO) 2008.
The authors highlight the importance of establishing this
diagnosis, even in pediatric age, to set the earliest possible a
strategy of clinical surveillance, prevention of associated complications
and the most adequate therapeutic approach.
Description
Keywords
Thrombocytosis essential thrombocythemia adolescent
Citation
Nascer e Crescer 2011; 20(4): 296-298