Serveur d'exploration sur le lymphœdème

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Primary upper‐limb lymphoedema

Identifieur interne : 003A72 ( Main/Curation ); précédent : 003A71; suivant : 003A73

Primary upper‐limb lymphoedema

Auteurs : S. Vignes [France] ; M. Arrault [France] ; A. Yannoutsos [France] ; M. Blanchard [France]

Source :

RBID : ISTEX:7A389B134574B6E403F0F9873D47945198B92F5A

Descripteurs français

English descriptors

Abstract

Summary Background  Lymphoedema is a general term used to designate pathological, regional accumulation of protein‐rich fluid. It can be either primary or secondary, and mainly occurs after cancer treatment.

Url:
DOI: 10.1111/bjd.12024

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ISTEX:7A389B134574B6E403F0F9873D47945198B92F5A

Le document en format XML

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<term>Adolescent</term>
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<term>Cellulite sous-cutanée</term>
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<div type="abstract">Summary Background  Lymphoedema is a general term used to designate pathological, regional accumulation of protein‐rich fluid. It can be either primary or secondary, and mainly occurs after cancer treatment.</div>
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<title level="j" type="main">British journal of dermatology : (1951)</title>
<title level="j" type="abbreviated">Br. j. dermatol. : (1951)</title>
<idno type="ISSN">0007-0963</idno>
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<date when="2013">2013</date>
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<title level="j" type="main">British journal of dermatology : (1951)</title>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Dermatology</term>
<term>Lymphedema</term>
<term>Upper limb</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Lymphoedème</term>
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<div type="abstract" xml:lang="en">Background Lymphoedema is a general term used to designate pathological, regional accumulation of protein-rich fluid. It can be either primary or secondary, and mainly occurs after cancer treatment. Objectives To analyse the clinical and lymphoscintigraphic characteristics of primary upper-limb lymphoedema (ULL). Methods All of the patients with ULL were recruited at a single Department of Lymphology between January 2007 and December 2011. Results In total, 60 patients (33 female, 27 male) were enrolled. For the 54 noncongenital lymphoedemas, the mean age at onset was 38.5 (range 3- 82) years. Lymphoedema was unilateral in 51 patients (85%). It always affected the hand, and less often the forearm (55%) or upper arm (23%). Eleven patients (18%) developed cellulitis after onset of lymphoedema, and 21 patients (35%) had associated lower-limb lymphoedema (LLL). Forty-six patients (with 49 lymphoedematous limbs) underwent lymphoscintigraphy: axillary lymph node uptake was diminished in 18 (37%), absent in 24 (49%) and normal in seven limbs (14%). Among the 43 patients with unilateral lymphoedema and lymphoscintigraphy, 28 had epitrochlear node visualization, suggesting a rerouting through the deep lymphatic system, with 15 only on the lymphoedematous limb and 22 on the contralateral nonlymphoedematous limb. The median follow-up period was 103 months, and 57/60 patients (95%) considered their lymphoedema to be stable. Conclusions Primary ULL appears later in life than LLL, without predominance in either sex. Infectious complications are rare and patients considered the lymphoedema volume stable throughout life.</div>
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<title level="a" type="main">Primary upper‐limb lymphoedema</title>
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<name sortKey="Vignes, S" sort="Vignes, S" uniqKey="Vignes S" first="S." last="Vignes">S. Vignes</name>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris</wicri:regionArea>
<placeName>
<region type="region" nuts="2">Île-de-France</region>
<settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Arrault, M" sort="Arrault, M" uniqKey="Arrault M" first="M." last="Arrault">M. Arrault</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris</wicri:regionArea>
<placeName>
<settlement type="city">Paris</settlement>
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<name sortKey="Yannoutsos, A" sort="Yannoutsos, A" uniqKey="Yannoutsos A" first="A." last="Yannoutsos">A. Yannoutsos</name>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris</wicri:regionArea>
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<settlement type="city">Paris</settlement>
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<wicri:regionArea>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris</wicri:regionArea>
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<title level="j" type="main">British Journal of Dermatology</title>
<title level="j" type="alt">BRITISH JOURNAL OF DERMATOLOGY</title>
<idno type="ISSN">0007-0963</idno>
<idno type="eISSN">1365-2133</idno>
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<date type="published" when="2013-02">2013-02</date>
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<idno type="ISSN">0007-0963</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Adolescent</term>
<term>Adult</term>
<term>Age of Onset</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Bandages</term>
<term>Cellulitis (complications)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Drainage (methods)</term>
<term>Female</term>
<term>Humans</term>
<term>Lymphedema (complications)</term>
<term>Lymphedema (diagnostic imaging)</term>
<term>Lymphedema (therapy)</term>
<term>Lymphoscintigraphy (methods)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Physical Therapy Modalities</term>
<term>Upper Extremity</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Bandages</term>
<term>Cellulite sous-cutanée ()</term>
<term>Drainage ()</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (imagerie diagnostique)</term>
<term>Lymphoscintigraphie ()</term>
<term>Membre supérieur</term>
<term>Mâle</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Techniques de physiothérapie</term>
<term>Âge de début</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Cellulitis</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en">
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr">
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Drainage</term>
<term>Lymphoscintigraphy</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en">
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adolescent</term>
<term>Adult</term>
<term>Age of Onset</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Bandages</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Physical Therapy Modalities</term>
<term>Upper Extremity</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Bandages</term>
<term>Cellulite sous-cutanée</term>
<term>Drainage</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Lymphoedème</term>
<term>Lymphoscintigraphie</term>
<term>Membre supérieur</term>
<term>Mâle</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Techniques de physiothérapie</term>
<term>Âge de début</term>
</keywords>
</textClass>
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</teiHeader>
<front>
<div type="abstract">Summary Background  Lymphoedema is a general term used to designate pathological, regional accumulation of protein‐rich fluid. It can be either primary or secondary, and mainly occurs after cancer treatment.</div>
</front>
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