Lymphangiosarcomata - experience in a lymphoedema clinic
Identifieur interne : 00CE90 ( Main/Merge ); précédent : 00CE89; suivant : 00CE91Lymphangiosarcomata - experience in a lymphoedema clinic
Auteurs : Paula M. Mulvenna ; Lydia Gillham ; Claud Fb RegnardSource :
- Palliative Medicine [ 0269-2163 ] ; 1995-01.
Descripteurs français
- KwdFr :
- Association thérapeutique, Bras, Cellulite sous-cutanée (), Cellulite sous-cutanée (anatomopathologie), Cellulite sous-cutanée (étiologie), Femelle, Humains, Issue fatale, Jambe, Lymphangiosarcome (), Lymphangiosarcome (anatomopathologie), Lymphangiosarcome (étiologie), Lymphoedème (), Lymphoedème (anatomopathologie), Maladie chronique, Sujet âgé, Sujet âgé de 80 ans ou plus.
- MESH :
- anatomopathologie : Cellulite sous-cutanée, Lymphangiosarcome, Lymphoedème.
- étiologie : Cellulite sous-cutanée, Lymphangiosarcome.
- Association thérapeutique, Bras, Cellulite sous-cutanée, Femelle, Humains, Issue fatale, Jambe, Lymphangiosarcome, Lymphoedème, Maladie chronique, Sujet âgé, Sujet âgé de 80 ans ou plus.
English descriptors
- KwdEn :
- Aged, Aged, 80 and over, Arm, Cellulitis (etiology), Cellulitis (pathology), Cellulitis (therapy), Chronic Disease, Combined Modality Therapy, Fatal Outcome, Female, Humans, Leg, Lymphangiosarcoma (etiology), Lymphangiosarcoma (pathology), Lymphangiosarcoma (therapy), Lymphedema (complications), Lymphedema (pathology), Lymphedema (therapy).
- MESH :
- complications : Lymphedema.
- etiology : Cellulitis, Lymphangiosarcoma.
- pathology : Cellulitis, Lymphangiosarcoma, Lymphedema.
- therapy : Cellulitis, Lymphangiosarcoma, Lymphedema.
- Aged, Aged, 80 and over, Arm, Chronic Disease, Combined Modality Therapy, Fatal Outcome, Female, Humans, Leg.
Abstract
Two cases of patients attending a lymphoedema clinic and developing lymphangiosarcomata are described. The epidemiology, natural history and management of this uncommon malignancy are discussed and the pertinent features that should be sought by professionals involved in routine follow-up of patients prone to lymphoedema outlined.
Url:
DOI: 10.1177/026921639500900108
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Mulvenna</name></author><author wicri:is="90%"><name sortKey="Gillham, Lydia" sort="Gillham, Lydia" uniqKey="Gillham L" first="Lydia" last="Gillham">Lydia Gillham</name></author><author wicri:is="90%"><name sortKey="Regnard, Claud Fb" sort="Regnard, Claud Fb" uniqKey="Regnard C" first="Claud Fb" last="Regnard">Claud Fb Regnard</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:4FF4307BEDFA0B287B3C10AE727327CCD2F36E7E</idno><date when="1995" year="1995">1995</date><idno type="doi">10.1177/026921639500900108</idno><idno type="url">https://api.istex.fr/document/4FF4307BEDFA0B287B3C10AE727327CCD2F36E7E/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">002469</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">002469</idno><idno type="wicri:Area/Istex/Curation">002469</idno><idno type="wicri:Area/Istex/Checkpoint">004831</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">004831</idno><idno type="wicri:doubleKey">0269-2163:1995:Mulvenna P:lymphangiosarcomata:experience:in</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Lymphangiosarcomata - experience in a lymphoedema clinic</title><author wicri:is="90%"><name sortKey="Mulvenna, Paula M" sort="Mulvenna, Paula M" uniqKey="Mulvenna P" first="Paula M" last="Mulvenna">Paula M. Mulvenna</name><affiliation><wicri:noCountry code="no comma">Senior Registrar Palliative Medicine</wicri:noCountry></affiliation></author><author wicri:is="90%"><name sortKey="Gillham, Lydia" sort="Gillham, Lydia" uniqKey="Gillham L" first="Lydia" last="Gillham">Lydia Gillham</name><affiliation><wicri:noCountry code="no comma">Senior Physiotherapist</wicri:noCountry></affiliation></author><author wicri:is="90%"><name sortKey="Regnard, Claud Fb" sort="Regnard, Claud Fb" uniqKey="Regnard C" first="Claud Fb" last="Regnard">Claud Fb Regnard</name><affiliation><wicri:noCountry code="subField">Tyne</wicri:noCountry></affiliation></author></analytic><monogr></monogr><series><title level="j">Palliative Medicine</title><idno type="ISSN">0269-2163</idno><idno type="eISSN">1477-030X</idno><imprint><publisher>Sage Publications</publisher><pubPlace>Sage CA: Thousand Oaks, CA</pubPlace><date type="published" when="1995-01">1995-01</date><biblScope unit="volume">9</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="55">55</biblScope><biblScope unit="page" to="59">59</biblScope></imprint><idno type="ISSN">0269-2163</idno></series><idno type="istex">4FF4307BEDFA0B287B3C10AE727327CCD2F36E7E</idno><idno type="DOI">10.1177/026921639500900108</idno><idno type="ArticleID">10.1177_026921639500900108</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0269-2163</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Two cases of patients attending a lymphoedema clinic and developing lymphangiosarcomata are described. The epidemiology, natural history and management of this uncommon malignancy are discussed and the pertinent features that should be sought by professionals involved in routine follow-up of patients prone to lymphoedema outlined.</div></front></TEI></ISTEX><PubMed><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Lymphangiosarcomata--experience in a lymphoedema clinic.</title><author><name sortKey="Mulvenna, P M" sort="Mulvenna, P M" uniqKey="Mulvenna P" first="P M" last="Mulvenna">P M Mulvenna</name><affiliation wicri:level="1"><nlm:affiliation>Department of Pharmacological Sciences, St Oswald's Hospice, Newcastle upon Tyne, UK.</nlm:affiliation><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Pharmacological Sciences, St Oswald's Hospice, Newcastle upon Tyne</wicri:regionArea><wicri:noRegion>Newcastle upon Tyne</wicri:noRegion></affiliation></author><author><name sortKey="Gillham, L" sort="Gillham, L" uniqKey="Gillham L" first="L" last="Gillham">L. Gillham</name></author><author><name sortKey="Regnard, C F" sort="Regnard, C F" uniqKey="Regnard C" first="C F" last="Regnard">C F Regnard</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1995">1995</date><idno type="RBID">pubmed:7719518</idno><idno type="pmid">7719518</idno><idno type="doi">10.1177/026921639500900108</idno><idno type="wicri:Area/PubMed/Corpus">005451</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">005451</idno><idno type="wicri:Area/PubMed/Curation">005451</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">005451</idno><idno type="wicri:Area/PubMed/Checkpoint">005451</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">005451</idno><idno type="wicri:Area/Ncbi/Merge">00B195</idno><idno type="wicri:Area/Ncbi/Curation">00B195</idno><idno type="wicri:Area/Ncbi/Checkpoint">00B195</idno><idno type="wicri:doubleKey">0269-2163:1995:Mulvenna P:lymphangiosarcomata:experience:in</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Lymphangiosarcomata--experience in a lymphoedema clinic.</title><author><name sortKey="Mulvenna, P M" sort="Mulvenna, P M" uniqKey="Mulvenna P" first="P M" last="Mulvenna">P M Mulvenna</name><affiliation wicri:level="1"><nlm:affiliation>Department of Pharmacological Sciences, St Oswald's Hospice, Newcastle upon Tyne, UK.</nlm:affiliation><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Pharmacological Sciences, St Oswald's Hospice, Newcastle upon Tyne</wicri:regionArea><wicri:noRegion>Newcastle upon Tyne</wicri:noRegion></affiliation></author><author><name sortKey="Gillham, L" sort="Gillham, L" uniqKey="Gillham L" first="L" last="Gillham">L. Gillham</name></author><author><name sortKey="Regnard, C F" sort="Regnard, C F" uniqKey="Regnard C" first="C F" last="Regnard">C F Regnard</name></author></analytic><series><title level="j">Palliative medicine</title><idno type="ISSN">0269-2163</idno><imprint><date when="1995" type="published">1995</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Aged, 80 and over</term><term>Arm</term><term>Cellulitis (etiology)</term><term>Cellulitis (pathology)</term><term>Cellulitis (therapy)</term><term>Chronic Disease</term><term>Combined Modality Therapy</term><term>Fatal Outcome</term><term>Female</term><term>Humans</term><term>Leg</term><term>Lymphangiosarcoma (etiology)</term><term>Lymphangiosarcoma (pathology)</term><term>Lymphangiosarcoma (therapy)</term><term>Lymphedema (complications)</term><term>Lymphedema (pathology)</term><term>Lymphedema (therapy)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Association thérapeutique</term><term>Bras</term><term>Cellulite sous-cutanée ()</term><term>Cellulite sous-cutanée (anatomopathologie)</term><term>Cellulite sous-cutanée (étiologie)</term><term>Femelle</term><term>Humains</term><term>Issue fatale</term><term>Jambe</term><term>Lymphangiosarcome ()</term><term>Lymphangiosarcome (anatomopathologie)</term><term>Lymphangiosarcome (étiologie)</term><term>Lymphoedème ()</term><term>Lymphoedème (anatomopathologie)</term><term>Maladie chronique</term><term>Sujet âgé</term><term>Sujet âgé de 80 ans ou plus</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Cellulite sous-cutanée</term><term>Lymphangiosarcome</term><term>Lymphoedème</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Cellulitis</term><term>Lymphangiosarcoma</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Cellulitis</term><term>Lymphangiosarcoma</term><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Cellulitis</term><term>Lymphangiosarcoma</term><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Cellulite sous-cutanée</term><term>Lymphangiosarcome</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Aged, 80 and over</term><term>Arm</term><term>Chronic Disease</term><term>Combined Modality Therapy</term><term>Fatal Outcome</term><term>Female</term><term>Humans</term><term>Leg</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Association thérapeutique</term><term>Bras</term><term>Cellulite sous-cutanée</term><term>Femelle</term><term>Humains</term><term>Issue fatale</term><term>Jambe</term><term>Lymphangiosarcome</term><term>Lymphoedème</term><term>Maladie chronique</term><term>Sujet âgé</term><term>Sujet âgé de 80 ans ou plus</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Two cases of patients attending a lymphoedema clinic and developing lymphangiosarcomata are described. The epidemiology, natural history and management of this uncommon malignancy are discussed and the pertinent features that should be sought by professionals involved in routine follow-up of patients prone to lymphoedema outlined.</div></front></TEI></PubMed></double></record>Pour manipuler ce document sous Unix (Dilib)
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