Primary upper‐limb lymphoedema
Identifieur interne : 003936 ( Istex/Curation ); précédent : 003935; suivant : 003937Primary upper‐limb lymphoedema
Auteurs : S. Vignes [France] ; M. Arrault [France] ; A. Yannoutsos [France] ; M. Blanchard [France]Source :
- British Journal of Dermatology [ 0007-0963 ] ; 2013-02.
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.
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DOI: 10.1111/bjd.12024
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Arrault</name><affiliation wicri:level="1"><mods:affiliation>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris, France</mods:affiliation><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></affiliation></author><author><name sortKey="Yannoutsos, A" sort="Yannoutsos, A" uniqKey="Yannoutsos A" first="A." last="Yannoutsos">A. 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Blanchard</name><affiliation wicri:level="1"><mods:affiliation>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris, France</mods:affiliation><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></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:7A389B134574B6E403F0F9873D47945198B92F5A</idno><date when="2013" year="2013">2013</date><idno type="doi">10.1111/bjd.12024</idno><idno type="url">https://api.istex.fr/document/7A389B134574B6E403F0F9873D47945198B92F5A/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">003936</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">003936</idno><idno type="wicri:Area/Istex/Curation">003936</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main">Primary upper‐limb lymphoedema</title><author><name sortKey="Vignes, S" sort="Vignes, S" uniqKey="Vignes S" first="S." last="Vignes">S. Vignes</name><affiliation wicri:level="1"><mods:affiliation>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris, France</mods:affiliation><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></affiliation></author><author><name sortKey="Arrault, M" sort="Arrault, M" uniqKey="Arrault M" first="M." last="Arrault">M. Arrault</name><affiliation wicri:level="1"><mods:affiliation>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris, France</mods:affiliation><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></affiliation></author><author><name sortKey="Yannoutsos, A" sort="Yannoutsos, A" uniqKey="Yannoutsos A" first="A." last="Yannoutsos">A. Yannoutsos</name><affiliation wicri:level="1"><mods:affiliation>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris, France</mods:affiliation><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></affiliation></author><author><name sortKey="Blanchard, M" sort="Blanchard, M" uniqKey="Blanchard M" first="M." last="Blanchard">M. Blanchard</name><affiliation wicri:level="1"><mods:affiliation>Department of Lymphology, Centre National de Référence des Maladies Vasculaires Rares (lymphœdèmes primaires), Hôpital Cognacq‐Jay, 75015 Paris, France</mods:affiliation><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></affiliation></author></analytic><monogr></monogr><series><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><imprint><biblScope unit="vol">168</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="272">272</biblScope><biblScope unit="page" to="276">276</biblScope><biblScope unit="page-count">5</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2013-02">2013-02</date></imprint><idno type="ISSN">0007-0963</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0007-0963</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></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></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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