LymphedemaV1, PubMed, Corpus, bibRecord, 006A62

[Primary lymphedema].

Identifieur interne : 006A62 ( PubMed/Corpus ); précédent : 006A61; suivant : 006A63

[Primary lymphedema].

Auteurs : A. Gregl ; D. Von Heyden ; F. Jentsch ; D. Yu

Source :

Zeitschrift fur Lymphologie. Journal of lymphology [ 0343-8554 ] ; 1983.

RBID : pubmed:6353789

English descriptors

KwdEn :
- Adolescent, Adult, Aging, Bacterial Infections (complications), Child, Child, Preschool, Elephantiasis (diagnosis), Elephantiasis (genetics), Female, Filariasis (complications), Hemangiosarcoma (complications), Humans, Lymphatic Metastasis, Lymphedema (classification), Lymphedema (diagnosis), Lymphedema (etiology), Male, Mycoses (complications), Thrombophlebitis (complications).
MESH :
- classification : Lymphedema.
- complications : Bacterial Infections, Filariasis, Hemangiosarcoma, Mycoses, Thrombophlebitis.
- diagnosis : Elephantiasis, Lymphedema.
- etiology : Lymphedema.
- genetics : Elephantiasis.
- Adolescent, Adult, Aging, Child, Child, Preschool, Female, Humans, Lymphatic Metastasis, Male.

Abstract

Secondary peripheral lymphedemas (all edemas based on pontine symptoms) are very much more frequent than primary edemas which are either congenital or due to a predisposition. Of the latter, only hereditary (essential) lymphedema and idiopathic lymphedema (lymphedema praecox) play a role in clinical practise with the regard to their incidence. The exceedingly rare hereditary lymphedemas, which differ from the primary noncongenital lymphedemas only with regard to the demonstrated heritability merely have a clinical significance. Thus for example only six such cases occurred amongst our patients in the last 20 years. Most primary lymphedemas occur at the time of puberty with a time span of 10 to 30 years. Primary lymphedemas can also occur within a genuine clinical picture (flat nevi, Recklinghausen disease etc.), so that underlying symptoms must be looked for when they occur.

PubMed: 6353789

Links to Exploration step

pubmed:6353789

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Primary lymphedema].</title>
<author><name sortKey="Gregl, A" sort="Gregl, A" uniqKey="Gregl A" first="A" last="Gregl">A. Gregl</name>
</author>
<author><name sortKey="Von Heyden, D" sort="Von Heyden, D" uniqKey="Von Heyden D" first="D" last="Von Heyden">D. Von Heyden</name>
</author>
<author><name sortKey="Jentsch, F" sort="Jentsch, F" uniqKey="Jentsch F" first="F" last="Jentsch">F. Jentsch</name>
</author>
<author><name sortKey="Yu, D" sort="Yu, D" uniqKey="Yu D" first="D" last="Yu">D. Yu</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1983">1983</date>
<idno type="RBID">pubmed:6353789</idno>
<idno type="pmid">6353789</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[Primary lymphedema].</title>
<author><name sortKey="Gregl, A" sort="Gregl, A" uniqKey="Gregl A" first="A" last="Gregl">A. Gregl</name>
</author>
<author><name sortKey="Von Heyden, D" sort="Von Heyden, D" uniqKey="Von Heyden D" first="D" last="Von Heyden">D. Von Heyden</name>
</author>
<author><name sortKey="Jentsch, F" sort="Jentsch, F" uniqKey="Jentsch F" first="F" last="Jentsch">F. Jentsch</name>
</author>
<author><name sortKey="Yu, D" sort="Yu, D" uniqKey="Yu D" first="D" last="Yu">D. Yu</name>
</author>
</analytic>
<series><title level="j">Zeitschrift fur Lymphologie. Journal of lymphology</title>
<idno type="ISSN">0343-8554</idno>
<imprint><date when="1983" type="published">1983</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Aging</term>
<term>Bacterial Infections (complications)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Elephantiasis (diagnosis)</term>
<term>Elephantiasis (genetics)</term>
<term>Female</term>
<term>Filariasis (complications)</term>
<term>Hemangiosarcoma (complications)</term>
<term>Humans</term>
<term>Lymphatic Metastasis</term>
<term>Lymphedema (classification)</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (etiology)</term>
<term>Male</term>
<term>Mycoses (complications)</term>
<term>Thrombophlebitis (complications)</term>
</keywords>
<keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Bacterial Infections</term>
<term>Filariasis</term>
<term>Hemangiosarcoma</term>
<term>Mycoses</term>
<term>Thrombophlebitis</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Elephantiasis</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Elephantiasis</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Aging</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Lymphatic Metastasis</term>
<term>Male</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Secondary peripheral lymphedemas (all edemas based on pontine symptoms) are very much more frequent than primary edemas which are either congenital or due to a predisposition. Of the latter, only hereditary (essential) lymphedema and idiopathic lymphedema (lymphedema praecox) play a role in clinical practise with the regard to their incidence. The exceedingly rare hereditary lymphedemas, which differ from the primary noncongenital lymphedemas only with regard to the demonstrated heritability merely have a clinical significance. Thus for example only six such cases occurred amongst our patients in the last 20 years. Most primary lymphedemas occur at the time of puberty with a time span of 10 to 30 years. Primary lymphedemas can also occur within a genuine clinical picture (flat nevi, Recklinghausen disease etc.), so that underlying symptoms must be looked for when they occur.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">6353789</PMID>
<DateCreated><Year>1983</Year>
<Month>11</Month>
<Day>23</Day>
</DateCreated>
<DateCompleted><Year>1983</Year>
<Month>11</Month>
<Day>23</Day>
</DateCompleted>
<DateRevised><Year>2008</Year>
<Month>02</Month>
<Day>26</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0343-8554</ISSN>
<JournalIssue CitedMedium="Print"><Volume>7</Volume>
<Issue>1</Issue>
<PubDate><Year>1983</Year>
<Month>Jul</Month>
</PubDate>
</JournalIssue>
<Title>Zeitschrift fur Lymphologie. Journal of lymphology</Title>
<ISOAbbreviation>Z Lymphol</ISOAbbreviation>
</Journal>
<ArticleTitle>[Primary lymphedema].</ArticleTitle>
<Pagination><MedlinePgn>21-8</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Secondary peripheral lymphedemas (all edemas based on pontine symptoms) are very much more frequent than primary edemas which are either congenital or due to a predisposition. Of the latter, only hereditary (essential) lymphedema and idiopathic lymphedema (lymphedema praecox) play a role in clinical practise with the regard to their incidence. The exceedingly rare hereditary lymphedemas, which differ from the primary noncongenital lymphedemas only with regard to the demonstrated heritability merely have a clinical significance. Thus for example only six such cases occurred amongst our patients in the last 20 years. Most primary lymphedemas occur at the time of puberty with a time span of 10 to 30 years. Primary lymphedemas can also occur within a genuine clinical picture (flat nevi, Recklinghausen disease etc.), so that underlying symptoms must be looked for when they occur.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gregl</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>von Heyden</LastName>
<ForeName>D</ForeName>
<Initials>D</Initials>
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<Author ValidYN="Y"><LastName>Jentsch</LastName>
<ForeName>F</ForeName>
<Initials>F</Initials>
</Author>
<Author ValidYN="Y"><LastName>Yu</LastName>
<ForeName>D</ForeName>
<Initials>D</Initials>
</Author>
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<Language>ger</Language>
<PublicationTypeList><PublicationType UI="D004740">English Abstract</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016454">Review</PublicationType>
</PublicationTypeList>
<VernacularTitle>Das primäre Lymphödem.</VernacularTitle>
</Article>
<MedlineJournalInfo><Country>Germany</Country>
<MedlineTA>Z Lymphol</MedlineTA>
<NlmUniqueID>7805527</NlmUniqueID>
<ISSNLinking>0343-8554</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000375" MajorTopicYN="N">Aging</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001424" MajorTopicYN="N">Bacterial Infections</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004604" MajorTopicYN="N">Elephantiasis</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005368" MajorTopicYN="N">Filariasis</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008207" MajorTopicYN="N">Lymphatic Metastasis</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000145" MajorTopicYN="Y">classification</QualifierName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009181" MajorTopicYN="N">Mycoses</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013924" MajorTopicYN="N">Thrombophlebitis</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
</MeshHeadingList>
<NumberOfReferences>33</NumberOfReferences>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1983</Year>
<Month>7</Month>
<Day>1</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>1983</Year>
<Month>7</Month>
<Day>1</Day>
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<PubMedPubDate PubStatus="entrez"><Year>1983</Year>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">6353789</ArticleId>
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</record>

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[Primary lymphedema].

[Primary lymphedema].

Source :

English descriptors

Abstract

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