Abstract |
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 muscular-skeletal hypertrophy of an extremity), and others with a high flow, such as the Parkes-Weber syndrome.
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Authors | P Redondo |
Journal | Anales del sistema sanitario de Navarra
(An Sist Sanit Navar)
Vol. 27 Suppl 1
Pg. 9-25
( 2004)
ISSN: 1137-6627 [Print] Spain |
Vernacular Title | Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural. |
PMID | 15148508
(Publication Type: English Abstract, Journal Article, Review)
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Topics |
- Arteriovenous Malformations
(classification, diagnosis)
- Blood Vessels
(abnormalities)
- Hemangioma
(classification, congenital, diagnosis)
- Humans
- Lymphatic Diseases
(classification, diagnosis)
- Neoplasms, Vascular Tissue
(classification, congenital, diagnosis)
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