[Limb lymphedema: Diagnosis, explorations, complications. French Lymphology Society].
Identifieur interne : 005F19 ( Main/Exploration ); précédent : 005F18; suivant : 005F20[Limb lymphedema: Diagnosis, explorations, complications. French Lymphology Society].
Auteurs : S. Vignes [France] ; M. Coupé ; F. Baulieu ; L. VaillantSource :
- Journal des maladies vasculaires [ 2214-8116 ] ; 2009.
Descripteurs français
- KwdFr :
- Adolescent, Adulte, Adulte d'âge moyen, Anthropométrie, Enfant, Facteurs de risque, Femelle, Humains, Lymphangiosarcome (étiologie), Lymphoedème (), Lymphoedème (diagnostic), Lymphoedème (génétique), Lymphoedème (imagerie diagnostique), Maladies chromosomiques (), Membres (anatomopathologie), Membres (physiopathologie), Mâle, Obésité (anatomopathologie), Qualité de vie, Scintigraphie, Sujet âgé, Tissu adipeux (anatomopathologie), Tumeurs (), Tumeurs cutanées (étiologie), Érysipèle (étiologie).
- MESH :
- anatomopathologie : Membres, Obésité, Tissu adipeux.
- diagnostic : Lymphoedème.
- génétique : Lymphoedème.
- imagerie diagnostique : Lymphoedème.
- physiopathologie : Membres.
- étiologie : Lymphangiosarcome, Tumeurs cutanées, Érysipèle.
- Adolescent, Adulte, Adulte d'âge moyen, Anthropométrie, Enfant, Facteurs de risque, Femelle, Humains, Lymphoedème, Maladies chromosomiques, Mâle, Qualité de vie, Scintigraphie, Sujet âgé, Tumeurs.
English descriptors
- KwdEn :
- Adipose Tissue (pathology), Adolescent, Adult, Aged, Anthropometry, Child, Chromosome Disorders (complications), Erysipelas (etiology), Extremities (pathology), Extremities (physiopathology), Female, Humans, Lymphangiosarcoma (etiology), Lymphedema (complications), Lymphedema (congenital), Lymphedema (diagnosis), Lymphedema (diagnostic imaging), Lymphedema (genetics), Lymphedema (therapy), Male, Middle Aged, Neoplasms (complications), Obesity (pathology), Quality of Life, Radionuclide Imaging, Risk Factors, Skin Neoplasms (etiology).
- MESH :
- complications : Chromosome Disorders, Lymphedema, Neoplasms.
- congenital : Lymphedema.
- diagnosis : Lymphedema.
- diagnostic imaging : Lymphedema.
- etiology : Erysipelas, Lymphangiosarcoma, Skin Neoplasms.
- genetics : Lymphedema.
- pathology : Adipose Tissue, Extremities, Obesity.
- physiopathology : Extremities.
- therapy : Lymphedema.
- Adolescent, Adult, Aged, Anthropometry, Child, Female, Humans, Male, Middle Aged, Quality of Life, Radionuclide Imaging, Risk Factors.
Abstract
Lymphedema results from impaired lymphatic transport with increased limb volume. Primary and secondary forms can be distinguished. Secondary lymphedema of the upper limb is the most frequent in France. A 2-cm difference on any segment of the limb confirms the diagnosis of lymphedema. Calculated lymphedema volume using the formula for a truncated cone is required to assess the efficacy of treatment and to monitor follow-up. Primary lymphedema is sporadic but rarely familial. Lymphoscintigraphy is useful in the primary form to evaluate precisely lymphatic function of the two limbs. Erysipelas is the main complication,but psychological or functional discomfort may occur throughout the course of lymphedema. Lipedema is the main differential diagnosis, defined as an abnormal accumulation of fat from hip to ankle and occurs almost exclusively in obese women.
PubMed: 20050179
Affiliations:
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Le document en format XML
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<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Anthropometry</term>
<term>Child</term>
<term>Chromosome Disorders (complications)</term>
<term>Erysipelas (etiology)</term>
<term>Extremities (pathology)</term>
<term>Extremities (physiopathology)</term>
<term>Female</term>
<term>Humans</term>
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<term>Lymphedema (complications)</term>
<term>Lymphedema (congenital)</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (diagnostic imaging)</term>
<term>Lymphedema (genetics)</term>
<term>Lymphedema (therapy)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neoplasms (complications)</term>
<term>Obesity (pathology)</term>
<term>Quality of Life</term>
<term>Radionuclide Imaging</term>
<term>Risk Factors</term>
<term>Skin Neoplasms (etiology)</term>
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<term>Enfant</term>
<term>Facteurs de risque</term>
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<term>Aged</term>
<term>Anthropometry</term>
<term>Child</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Quality of Life</term>
<term>Radionuclide Imaging</term>
<term>Risk Factors</term>
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<term>Adulte d'âge moyen</term>
<term>Anthropométrie</term>
<term>Enfant</term>
<term>Facteurs de risque</term>
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<term>Maladies chromosomiques</term>
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<front><div type="abstract" xml:lang="en">Lymphedema results from impaired lymphatic transport with increased limb volume. Primary and secondary forms can be distinguished. Secondary lymphedema of the upper limb is the most frequent in France. A 2-cm difference on any segment of the limb confirms the diagnosis of lymphedema. Calculated lymphedema volume using the formula for a truncated cone is required to assess the efficacy of treatment and to monitor follow-up. Primary lymphedema is sporadic but rarely familial. Lymphoscintigraphy is useful in the primary form to evaluate precisely lymphatic function of the two limbs. Erysipelas is the main complication,but psychological or functional discomfort may occur throughout the course of lymphedema. Lipedema is the main differential diagnosis, defined as an abnormal accumulation of fat from hip to ankle and occurs almost exclusively in obese women.</div>
</front>
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