Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural

Vascular anomalies are divided into tumours and malformations. Haemangiomas are the most frequent amongst the former. Not normally present at birth, except in a premonitory form, they grow for 10-12 months due to hyperplasia, to subsequently undergo a progressive involution for a period that might l...

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Autor: Redondo-Bellón, P. (Pedro)|||/items/c82abb7b-9e9c-4498-a2fd-aac715171930
Tipo de recurso: artículo
Fecha de publicación:2004
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:español
OAI Identifier:oai:dadun.unav.edu:10171/22698
Acceso en línea:https://hdl.handle.net/10171/22698
Access Level:acceso abierto
Palabra clave:Haemangioma
Vascular malformation
Classification
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spelling Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia naturalClassification of vascular anomalies (tumours and malformations). Clinical characteristics and natural historyRedondo-Bellón, P. (Pedro)|||/items/c82abb7b-9e9c-4498-a2fd-aac715171930HaemangiomaVascular malformationClassificationVascular anomalies are divided into tumours and malformations. Haemangiomas are the most frequent amongst the former. Not normally present at birth, except in a premonitory form, they grow for 10-12 months due to hyperplasia, to subsequently undergo a progressive involution for a period that might last from ten to twelve years. They have an incidence of up to 12% in newborns; they are more common amongst girls; and are divided into superficial, deep and compound. Congenital haemangiomas and those that do not undergo involution are considered to be rare entities. Vascular malformations, with a lower incidence than haemangiomas, are always present at birth, they grow by hypertrophy and never undergo involution. According to the classification of the ISSVA, vascular malformations are divided - depending on the vessel affected - into capillary or venular (port-wine stain), venous, lymphatic, arteriovenous and combined or complex. Each of these has certain defining clinical and haemodynamic peculiarities. Within the final group are included some with a low flow, such as the Klippel-Trenaunay syndrome (venous and lymphatic venular vascular malformation associated with the muscularskeletal hypertrophy of an extremity), and others with a high flow, such as the Parkes-Weber syndrome.Gobierno de Navarra. Departamento de SaludDadun. Depósito Académico Digital Universidad de Navarra20122012-06-2220042004-01-0120042004-01-01journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10171/22698reponame:Dadun. Depósito Académico Digital de la Universidad de Navarrainstname:Universidad de NavarraEspañolspaopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:dadun.unav.edu:10171/226982026-06-21T12:47:57Z
dc.title.none.fl_str_mv Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
Classification of vascular anomalies (tumours and malformations). Clinical characteristics and natural history
title Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
spellingShingle Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
Redondo-Bellón, P. (Pedro)|||/items/c82abb7b-9e9c-4498-a2fd-aac715171930
Haemangioma
Vascular malformation
Classification
title_short Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
title_full Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
title_fullStr Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
title_full_unstemmed Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
title_sort Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural
dc.creator.none.fl_str_mv Redondo-Bellón, P. (Pedro)|||/items/c82abb7b-9e9c-4498-a2fd-aac715171930
author Redondo-Bellón, P. (Pedro)|||/items/c82abb7b-9e9c-4498-a2fd-aac715171930
author_facet Redondo-Bellón, P. (Pedro)|||/items/c82abb7b-9e9c-4498-a2fd-aac715171930
author_role author
dc.contributor.none.fl_str_mv Dadun. Depósito Académico Digital Universidad de Navarra
dc.subject.none.fl_str_mv Haemangioma
Vascular malformation
Classification
topic Haemangioma
Vascular malformation
Classification
description Vascular anomalies are divided into tumours and malformations. Haemangiomas are the most frequent amongst the former. Not normally present at birth, except in a premonitory form, they grow for 10-12 months due to hyperplasia, to subsequently undergo a progressive involution for a period that might last from ten to twelve years. They have an incidence of up to 12% in newborns; they are more common amongst girls; and are divided into superficial, deep and compound. Congenital haemangiomas and those that do not undergo involution are considered to be rare entities. Vascular malformations, with a lower incidence than haemangiomas, are always present at birth, they grow by hypertrophy and never undergo involution. According to the classification of the ISSVA, vascular malformations are divided - depending on the vessel affected - into capillary or venular (port-wine stain), venous, lymphatic, arteriovenous and combined or complex. Each of these has certain defining clinical and haemodynamic peculiarities. Within the final group are included some with a low flow, such as the Klippel-Trenaunay syndrome (venous and lymphatic venular vascular malformation associated with the muscularskeletal hypertrophy of an extremity), and others with a high flow, such as the Parkes-Weber syndrome.
publishDate 2004
dc.date.none.fl_str_mv 2004
2004-01-01
2004
2004-01-01
2012
2012-06-22
dc.type.none.fl_str_mv journal article
http://purl.org/coar/resource_type/c_6501
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/10171/22698
url https://hdl.handle.net/10171/22698
dc.language.none.fl_str_mv Español
spa
language_invalid_str_mv Español
language spa
dc.rights.none.fl_str_mv open access
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dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
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eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Gobierno de Navarra. Departamento de Salud
publisher.none.fl_str_mv Gobierno de Navarra. Departamento de Salud
dc.source.none.fl_str_mv reponame:Dadun. Depósito Académico Digital de la Universidad de Navarra
instname:Universidad de Navarra
instname_str Universidad de Navarra
reponame_str Dadun. Depósito Académico Digital de la Universidad de Navarra
collection Dadun. Depósito Académico Digital de la Universidad de Navarra
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