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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Autores principales: Molinos-Castro,Sonia, Pesqueira-Fontán,Paula María, Díaz-Peromingo,José Antonio
Lenguaje:Spanish / Castilian
Publicado: Sociedad Médica de Santiago 2009
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872009000500015
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spelling 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
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