[Limb lymphedema: Diagnosis, explorations, complications. French Lymphology Society].
Identifieur interne : 002C18 ( PubMed/Corpus ); précédent : 002C17; suivant : 002C19[Limb lymphedema: Diagnosis, explorations, complications. French Lymphology Society].
Auteurs : S. Vignes ; M. Coupé ; F. Baulieu ; L. VaillantSource :
- Journal des maladies vasculaires [ 2214-8116 ] ; 2009.
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
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pubmed:20050179Le document en format XML
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Vaillant</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2009">2009</date><idno type="RBID">pubmed:20050179</idno><idno type="pmid">20050179</idno><idno type="wicri:Area/PubMed/Corpus">002C18</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002C18</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">[Limb lymphedema: Diagnosis, explorations, complications. French Lymphology Society].</title><author><name sortKey="Vignes, S" sort="Vignes, S" uniqKey="Vignes S" first="S" last="Vignes">S. Vignes</name><affiliation><nlm:affiliation>Unité de lymphologie, hôpital Cognacq-Jay, Centre national de référence des maladies vasculaires rares, 15, rue Eugène-Millon,75015 Paris, France.</nlm:affiliation></affiliation></author><author><name sortKey="Coupe, M" sort="Coupe, M" uniqKey="Coupe M" first="M" last="Coupé">M. Coupé</name></author><author><name sortKey="Baulieu, F" sort="Baulieu, F" uniqKey="Baulieu F" first="F" last="Baulieu">F. Baulieu</name></author><author><name sortKey="Vaillant, L" sort="Vaillant, L" uniqKey="Vaillant L" first="L" last="Vaillant">L. Vaillant</name></author></analytic><series><title level="j">Journal des maladies vasculaires</title><idno type="eISSN">2214-8116</idno><imprint><date when="2009" type="published">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adipose Tissue (pathology)</term><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><term>Lymphangiosarcoma (etiology)</term><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></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Chromosome Disorders</term><term>Lymphedema</term><term>Neoplasms</term></keywords><keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Erysipelas</term><term>Lymphangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Adipose Tissue</term><term>Extremities</term><term>Obesity</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Extremities</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>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></keywords></textClass></profileDesc></teiHeader><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></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20050179</PMID><DateCreated><Year>2009</Year><Month>12</Month><Day>18</Day></DateCreated><DateCompleted><Year>2010</Year><Month>03</Month><Day>16</Day></DateCompleted><DateRevised><Year>2016</Year><Month>11</Month><Day>25</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">2214-8116</ISSN><JournalIssue CitedMedium="Internet"><Volume>34</Volume><Issue>5</Issue><PubDate><Year>2009</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Journal des maladies vasculaires</Title><ISOAbbreviation>J Mal Vasc</ISOAbbreviation></Journal><ArticleTitle>[Limb lymphedema: Diagnosis, explorations, complications. French Lymphology Society].</ArticleTitle><Pagination><MedlinePgn>314-22</MedlinePgn></Pagination><Abstract><AbstractText>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.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Vignes</LastName><ForeName>S</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Unité de lymphologie, hôpital Cognacq-Jay, Centre national de référence des maladies vasculaires rares, 15, rue Eugène-Millon,75015 Paris, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Coupé</LastName><ForeName>M</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Baulieu</LastName><ForeName>F</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Vaillant</LastName><ForeName>L</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><CollectiveName>Groupe Recommandations de la Société Française de Lymphologie</CollectiveName></Author></AuthorList><Language>fre</Language><PublicationTypeList><PublicationType UI="D016446">Consensus Development Conference</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D017065">Practice Guideline</PublicationType></PublicationTypeList><VernacularTitle>Les lymphoedèmes des membres: diagnostic, explorations, complications.</VernacularTitle></Article><MedlineJournalInfo><Country>France</Country><MedlineTA>J Mal Vasc</MedlineTA><NlmUniqueID>7707965</NlmUniqueID><ISSNLinking>0398-0499</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000273" MajorTopicYN="N">Adipose Tissue</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000886" MajorTopicYN="N">Anthropometry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D025063" MajorTopicYN="N">Chromosome Disorders</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004886" MajorTopicYN="N">Erysipelas</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005121" MajorTopicYN="N">Extremities</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="Y">Lymphedema</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000151" MajorTopicYN="N">congenital</QualifierName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009369" MajorTopicYN="N">Neoplasms</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009765" MajorTopicYN="N">Obesity</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011788" MajorTopicYN="N">Quality of Life</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011877" MajorTopicYN="N">Radionuclide Imaging</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012307" MajorTopicYN="N">Risk Factors</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName></MeshHeading></MeshHeadingList><NumberOfReferences>53</NumberOfReferences></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2010</Year><Month>1</Month><Day>6</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2010</Year><Month>1</Month><Day>6</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2010</Year><Month>3</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">20050179</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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