Telangiectasia hemorrágica hereditaria: Tratamiento farmacológico
Hereditary hemorrhagic telangiectasia (HHT) of Rendu-Osler-Weber disease is a multi system vascular dysplasia characterized by the presence of multiple telangiectasias, mainly affecting mucosal tissue and arterial-venous connections. It commonly affects lungs, liver and central nervous system. Bleed...
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Lenguaje: | Spanish / Castilian |
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Sociedad Médica de Santiago
2009
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oai:scielo:S0034-988720090005000152009-07-17Telangiectasia hemorrágica hereditaria: Tratamiento farmacológicoMolinos-Castro,SoniaPesqueira-Fontán,Paula MaríaDíaz-Peromingo,José Antonio Blood transfusions Fibrinolysis Telangiectasia, hereditary hemorrhagic Hereditary hemorrhagic telangiectasia (HHT) of Rendu-Osler-Weber disease is a multi system vascular dysplasia characterized by the presence of multiple telangiectasias, mainly affecting mucosal tissue and arterial-venous connections. It commonly affects lungs, liver and central nervous system. Bleeding is the most common symptom and its treatment can be surgical or pharmacological. We herein review the systemic therapy that attempts to minimize bleeding as well as blood transfusion therapy. Blood therapy and fibrinolytic treatment especially aminocaproic acid and tranexamic acid are discussed. Danazol, hormone therapy and other less common drugs used in the treatment of HHT are also reviewed.info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.137 n.5 20092009-05-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872009000500015es10.4067/S0034-98872009000500015 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
Spanish / Castilian |
topic |
Blood transfusions Fibrinolysis Telangiectasia, hereditary hemorrhagic |
spellingShingle |
Blood transfusions Fibrinolysis Telangiectasia, hereditary hemorrhagic Molinos-Castro,Sonia Pesqueira-Fontán,Paula María Díaz-Peromingo,José Antonio Telangiectasia hemorrágica hereditaria: Tratamiento farmacológico |
description |
Hereditary hemorrhagic telangiectasia (HHT) of Rendu-Osler-Weber disease is a multi system vascular dysplasia characterized by the presence of multiple telangiectasias, mainly affecting mucosal tissue and arterial-venous connections. It commonly affects lungs, liver and central nervous system. Bleeding is the most common symptom and its treatment can be surgical or pharmacological. We herein review the systemic therapy that attempts to minimize bleeding as well as blood transfusion therapy. Blood therapy and fibrinolytic treatment especially aminocaproic acid and tranexamic acid are discussed. Danazol, hormone therapy and other less common drugs used in the treatment of HHT are also reviewed. |
author |
Molinos-Castro,Sonia Pesqueira-Fontán,Paula María Díaz-Peromingo,José Antonio |
author_facet |
Molinos-Castro,Sonia Pesqueira-Fontán,Paula María Díaz-Peromingo,José Antonio |
author_sort |
Molinos-Castro,Sonia |
title |
Telangiectasia hemorrágica hereditaria: Tratamiento farmacológico |
title_short |
Telangiectasia hemorrágica hereditaria: Tratamiento farmacológico |
title_full |
Telangiectasia hemorrágica hereditaria: Tratamiento farmacológico |
title_fullStr |
Telangiectasia hemorrágica hereditaria: Tratamiento farmacológico |
title_full_unstemmed |
Telangiectasia hemorrágica hereditaria: Tratamiento farmacológico |
title_sort |
telangiectasia hemorrágica hereditaria: tratamiento farmacológico |
publisher |
Sociedad Médica de Santiago |
publishDate |
2009 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872009000500015 |
work_keys_str_mv |
AT molinoscastrosonia telangiectasiahemorragicahereditariatratamientofarmacologico AT pesqueirafontanpaulamaria telangiectasiahemorragicahereditariatratamientofarmacologico AT diazperomingojoseantonio telangiectasiahemorragicahereditariatratamientofarmacologico |
_version_ |
1718436444468412416 |