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Caso hematológico: trombocitemia essencial

dc.contributor.authorLopes, R.
dc.contributor.authorAraújo, L.
dc.contributor.authorCosta, E.
dc.contributor.authorSoares, S.
dc.contributor.authorBarbot, J.
dc.date.accessioned2012-08-28T12:12:01Z
dc.date.available2012-08-28T12:12:01Z
dc.date.issued2011-12
dc.description.abstractEssential 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.por
dc.identifier.citationNascer e Crescer 2011; 20(4): 296-298por
dc.identifier.issn0872-0754
dc.identifier.urihttp://hdl.handle.net/10400.16/1302
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherNascer e Crescerpor
dc.subjectThrombocytosispor
dc.subjectessential thrombocythemiapor
dc.subjectadolescentpor
dc.titleCaso hematológico: trombocitemia essencialpor
dc.title.alternativeHematologic case: essential thrombocythemiapor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.endPage298por
oaire.citation.issue20(4)por
oaire.citation.startPage296por
oaire.citation.titleNascer e Crescerpor
oaire.citation.volume20por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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