Trombocitemia Essencial

Essential thrombocythaemia is a chronic myeloproliferative disorder characterized by the proliferation of megakaryocytes in the bone marrow, leading to a persistent increase in circulating platelets. Apart from this increase (>600 x 10(9)/L) this disease also exhibits accentuated hyperplasia of the megakaryocytes in the bone marrow, splenomegaly and clinically both thrombotic and haemorrhagic episodes. The etiology of this illness is largely unknown and the clinical manifestations are mostly asymptomatic, thus the diagnostic is often accidentally made. Here the case report of a 71-year-old male patient is discussed, who was admitted into hospital due to occlusion of the femoral artery requiring re-vascularisation. The physical exam showed that the patient suffered several other symptoms related to essential thrombocythaemia. In conclusion, this is a grave, potentially fatal disease which needs further study to determine the etiology. Early diagnosis and treatment are crucial for a good prognosis.

Saved in:
Bibliographic Details
Main Authors: Leite,Andrea B., Silva,Herivaldo F., Nogueira,Otho L.
Format: Digital revista
Language:Portuguese
Published: Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular 2001
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842001000100007
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S1516-84842001000100007
record_format ojs
spelling oai:scielo:S1516-848420010001000072003-06-12Trombocitemia EssencialLeite,Andrea B.Silva,Herivaldo F.Nogueira,Otho L.Essential thrombocythaemia is a chronic myeloproliferative disorder characterized by the proliferation of megakaryocytes in the bone marrow, leading to a persistent increase in circulating platelets. Apart from this increase (>600 x 10(9)/L) this disease also exhibits accentuated hyperplasia of the megakaryocytes in the bone marrow, splenomegaly and clinically both thrombotic and haemorrhagic episodes. The etiology of this illness is largely unknown and the clinical manifestations are mostly asymptomatic, thus the diagnostic is often accidentally made. Here the case report of a 71-year-old male patient is discussed, who was admitted into hospital due to occlusion of the femoral artery requiring re-vascularisation. The physical exam showed that the patient suffered several other symptoms related to essential thrombocythaemia. In conclusion, this is a grave, potentially fatal disease which needs further study to determine the etiology. Early diagnosis and treatment are crucial for a good prognosis.info:eu-repo/semantics/openAccessAssociação Brasileira de Hematologia e Hemoterapia e Terapia CelularRevista Brasileira de Hematologia e Hemoterapia v.23 n.1 20012001-04-01info:eu-repo/semantics/othertext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842001000100007pt10.1590/S1516-84842001000100007
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language Portuguese
format Digital
author Leite,Andrea B.
Silva,Herivaldo F.
Nogueira,Otho L.
spellingShingle Leite,Andrea B.
Silva,Herivaldo F.
Nogueira,Otho L.
Trombocitemia Essencial
author_facet Leite,Andrea B.
Silva,Herivaldo F.
Nogueira,Otho L.
author_sort Leite,Andrea B.
title Trombocitemia Essencial
title_short Trombocitemia Essencial
title_full Trombocitemia Essencial
title_fullStr Trombocitemia Essencial
title_full_unstemmed Trombocitemia Essencial
title_sort trombocitemia essencial
description Essential thrombocythaemia is a chronic myeloproliferative disorder characterized by the proliferation of megakaryocytes in the bone marrow, leading to a persistent increase in circulating platelets. Apart from this increase (>600 x 10(9)/L) this disease also exhibits accentuated hyperplasia of the megakaryocytes in the bone marrow, splenomegaly and clinically both thrombotic and haemorrhagic episodes. The etiology of this illness is largely unknown and the clinical manifestations are mostly asymptomatic, thus the diagnostic is often accidentally made. Here the case report of a 71-year-old male patient is discussed, who was admitted into hospital due to occlusion of the femoral artery requiring re-vascularisation. The physical exam showed that the patient suffered several other symptoms related to essential thrombocythaemia. In conclusion, this is a grave, potentially fatal disease which needs further study to determine the etiology. Early diagnosis and treatment are crucial for a good prognosis.
publisher Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
publishDate 2001
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842001000100007
work_keys_str_mv AT leiteandreab trombocitemiaessencial
AT silvaherivaldof trombocitemiaessencial
AT nogueiraothol trombocitemiaessencial
_version_ 1756423368215625728