LymphedemaV1, France, Analysis, bibRecord, 000A89

[The lymphatic malformations: clinical aspects and evolution].

Identifieur interne : 000A89 ( France/Analysis ); précédent : 000A88; suivant : 000A90

[The lymphatic malformations: clinical aspects and evolution].

Auteurs : B. Salazard [France] ; J. Londner ; D. Casanova ; J. Bardot ; G. Magalon

Source :

Annales de chirurgie plastique et esthetique [ 0294-1260 ]

RBID : pubmed:17007978

Descripteurs français

KwdFr :
- Aisselle (anatomopathologie), Cou (anatomopathologie), Enchondromatose (diagnostic), Facteurs de l'âge, Humains, Lymphoedème (), Lymphoedème (diagnostic), Malformations lymphatiques (), Malformations lymphatiques (diagnostic), Nouveau-né, Puberté (physiologie), Syndrome de Klippel-Trénaunay (diagnostic), Vaisseaux lymphatiques (malformations), Vaisseaux sanguins (malformations).
MESH :
- anatomopathologie : Aisselle, Cou.
- diagnostic : Enchondromatose, Lymphoedème, Malformations lymphatiques, Syndrome de Klippel-Trénaunay.
- malformations : Vaisseaux lymphatiques, Vaisseaux sanguins.
- physiologie : Puberté.
- Facteurs de l'âge, Humains, Lymphoedème, Malformations lymphatiques, Nouveau-né.

English descriptors

KwdEn :
- Age Factors, Axilla (pathology), Blood Vessels (abnormalities), Enchondromatosis (diagnosis), Humans, Infant, Newborn, Klippel-Trenaunay-Weber Syndrome (diagnosis), Lymphatic Abnormalities (classification), Lymphatic Abnormalities (diagnosis), Lymphatic Vessels (abnormalities), Lymphedema (congenital), Lymphedema (diagnosis), Neck (pathology), Puberty (physiology).
MESH :
- abnormalities : Blood Vessels, Lymphatic Vessels.
- classification : Lymphatic Abnormalities.
- congenital : Lymphedema.
- diagnosis : Enchondromatosis, Klippel-Trenaunay-Weber Syndrome, Lymphatic Abnormalities, Lymphedema.
- pathology : Axilla, Neck.
- physiology : Puberty.
- Age Factors, Humans, Infant, Newborn.

Abstract

Lymphatic malformations (LM) are the most frequent vascular malformations. There are three types of lesions involving lymphatic development that must be included in LM: vascular anomalies and knots (truncal malformations [TLM]); cystic anomalies, superficial or deep, uni- or multicystic (extratruncal malformations [ETLM]) and hemolymphatic anomalies which combine venous, arterial, or capillary malformations with LM. ETLM can be ubiquitously distributed but most are located in the cervical or axillary regions. Most ETLM are diagnosed at birth and in 80-90% of the cases before the age of 2. The clinical aspects are extremely variable: superficial ETLM (vesicular) and deep ETLM, localised or diffuse, mono- or multicystic. TLM are generally located on a lower limb with neonatal lymphatic oedema (often in a polymalformation context). All forms of the hemolymphatic combination can be identified. They are generally located on the limbs and are often unilateral. They are usually sporadic but can also be can be found in polymalformation syndromes (Klippel-Trénaunay, Parkes-Weber, Protée, Maffucci). ETLM generally tend to increase in volume and spread with age with stabilisation at puberty. They do not tend to spontaneously regress. Specific local complications can have serious consequences. They are linked to haemorrhaging, infections and compression phenomena. There can also be complications such as skeletal and soft tissue hypertrophy.

DOI: 10.1016/j.anplas.2006.07.010
PubMed: 17007978

Affiliations:

Links to Exploration step

pubmed:17007978

Le document en format XML

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<term>Enchondromatosis (diagnosis)</term>
<term>Humans</term>
<term>Infant, Newborn</term>
<term>Klippel-Trenaunay-Weber Syndrome (diagnosis)</term>
<term>Lymphatic Abnormalities (classification)</term>
<term>Lymphatic Abnormalities (diagnosis)</term>
<term>Lymphatic Vessels (abnormalities)</term>
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<term>Lymphedema (diagnosis)</term>
<term>Neck (pathology)</term>
<term>Puberty (physiology)</term>
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<term>Facteurs de l'âge</term>
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<term>Lymphedema</term>
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<front><div type="abstract" xml:lang="en">Lymphatic malformations (LM) are the most frequent vascular malformations. There are three types of lesions involving lymphatic development that must be included in LM: vascular anomalies and knots (truncal malformations [TLM]); cystic anomalies, superficial or deep, uni- or multicystic (extratruncal malformations [ETLM]) and hemolymphatic anomalies which combine venous, arterial, or capillary malformations with LM. ETLM can be ubiquitously distributed but most are located in the cervical or axillary regions. Most ETLM are diagnosed at birth and in 80-90% of the cases before the age of 2. The clinical aspects are extremely variable: superficial ETLM (vesicular) and deep ETLM, localised or diffuse, mono- or multicystic. TLM are generally located on a lower limb with neonatal lymphatic oedema (often in a polymalformation context). All forms of the hemolymphatic combination can be identified. They are generally located on the limbs and are often unilateral. They are usually sporadic but can also be can be found in polymalformation syndromes (Klippel-Trénaunay, Parkes-Weber, Protée, Maffucci). ETLM generally tend to increase in volume and spread with age with stabilisation at puberty. They do not tend to spontaneously regress. Specific local complications can have serious consequences. They are linked to haemorrhaging, infections and compression phenomena. There can also be complications such as skeletal and soft tissue hypertrophy.</div>
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Serveur d'exploration sur le lymphœdème

[The lymphatic malformations: clinical aspects and evolution].

[The lymphatic malformations: clinical aspects and evolution].

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki

	Serveur d'exploration sur le lymphœdème
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