LymphedemaV1, Ncbi, Merge, bibRecord, 00B195

Lymphangiosarcomata--experience in a lymphoedema clinic.

Identifieur interne : 00B195 ( Ncbi/Merge ); précédent : 00B194; suivant : 00B196

Lymphangiosarcomata--experience in a lymphoedema clinic.

Auteurs : P M Mulvenna [Royaume-Uni] ; L. Gillham ; C F Regnard

Source :

Palliative medicine [ 0269-2163 ] ; 1995.

RBID : pubmed:7719518

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.

DOI: 10.1177/026921639500900108
PubMed: 7719518

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pubmed:7719518

Le document en format XML

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<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>
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<author><name sortKey="Gillham, L" sort="Gillham, L" uniqKey="Gillham L" first="L" last="Gillham">L. Gillham</name>
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<author><name sortKey="Regnard, C F" sort="Regnard, C F" uniqKey="Regnard C" first="C F" last="Regnard">C F Regnard</name>
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<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>
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<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>
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</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><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">7719518</PMID>
<DateCreated><Year>1995</Year>
<Month>05</Month>
<Day>25</Day>
</DateCreated>
<DateCompleted><Year>1995</Year>
<Month>05</Month>
<Day>25</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>02</Month>
<Day>14</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0269-2163</ISSN>
<JournalIssue CitedMedium="Print"><Volume>9</Volume>
<Issue>1</Issue>
<PubDate><Year>1995</Year>
<Month>Jan</Month>
</PubDate>
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<Title>Palliative medicine</Title>
<ISOAbbreviation>Palliat Med</ISOAbbreviation>
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<ArticleTitle>Lymphangiosarcomata--experience in a lymphoedema clinic.</ArticleTitle>
<Pagination><MedlinePgn>55-9</MedlinePgn>
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<Abstract><AbstractText>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.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mulvenna</LastName>
<ForeName>P M</ForeName>
<Initials>PM</Initials>
<AffiliationInfo><Affiliation>Department of Pharmacological Sciences, St Oswald's Hospice, Newcastle upon Tyne, UK.</Affiliation>
</AffiliationInfo>
</Author>
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<Author ValidYN="Y"><LastName>Regnard</LastName>
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<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
<QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName>
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<MeshHeading><DescriptorName UI="D002908" MajorTopicYN="N">Chronic Disease</DescriptorName>
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<MeshHeading><DescriptorName UI="D003131" MajorTopicYN="N">Combined Modality Therapy</DescriptorName>
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<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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</MeshHeading>
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<MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName>
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<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
<QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
<QualifierName UI="Q000628" MajorTopicYN="Y">therapy</QualifierName>
</MeshHeading>
</MeshHeadingList>
<NumberOfReferences>11</NumberOfReferences>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1995</Year>
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<Day>1</Day>
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Lymphangiosarcomata--experience in a lymphoedema clinic.

Lymphangiosarcomata--experience in a lymphoedema clinic.

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