[Primary lymphedema].
Identifieur interne : 006073 ( PubMed/Checkpoint ); précédent : 006072; suivant : 006074[Primary lymphedema].
Auteurs : A. Gregl ; D. Von Heyden ; F. Jentsch ; D. YuSource :
- Zeitschrift fur Lymphologie. Journal of lymphology [ 0343-8554 ] ; 1983.
Descripteurs français
- KwdFr :
- Adolescent, Adulte, Enfant, Enfant d'âge préscolaire, Femelle, Filarioses (), Humains, Hémangiosarcome (), Infections bactériennes (), Lymphoedème (), Lymphoedème (diagnostic), Lymphoedème (étiologie), Mycoses (), Mâle, Métastase lymphatique, Thrombophlébite (), Vieillissement, Éléphantiasis (diagnostic), Éléphantiasis (génétique).
- MESH :
- diagnostic : Lymphoedème, Éléphantiasis.
- génétique : Éléphantiasis.
- étiologie : Lymphoedème.
- Adolescent, Adulte, Enfant, Enfant d'âge préscolaire, Femelle, Filarioses, Humains, Hémangiosarcome, Infections bactériennes, Lymphoedème, Mycoses, Mâle, Métastase lymphatique, Thrombophlébite, Vieillissement.
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
Affiliations:
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pubmed:6353789Le document en format XML
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<author><name sortKey="Von Heyden, D" sort="Von Heyden, D" uniqKey="Von Heyden D" first="D" last="Von Heyden">D. Von Heyden</name>
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<author><name sortKey="Jentsch, F" sort="Jentsch, F" uniqKey="Jentsch F" first="F" last="Jentsch">F. Jentsch</name>
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<author><name sortKey="Yu, D" sort="Yu, D" uniqKey="Yu D" first="D" last="Yu">D. Yu</name>
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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="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Filarioses ()</term>
<term>Humains</term>
<term>Hémangiosarcome ()</term>
<term>Infections bactériennes ()</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (étiologie)</term>
<term>Mycoses ()</term>
<term>Mâle</term>
<term>Métastase lymphatique</term>
<term>Thrombophlébite ()</term>
<term>Vieillissement</term>
<term>Éléphantiasis (diagnostic)</term>
<term>Éléphantiasis (génétique)</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="diagnostic" xml:lang="fr"><term>Lymphoedème</term>
<term>Éléphantiasis</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Elephantiasis</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Éléphantiasis</term>
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<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Lymphoedème</term>
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<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>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Filarioses</term>
<term>Humains</term>
<term>Hémangiosarcome</term>
<term>Infections bactériennes</term>
<term>Lymphoedème</term>
<term>Mycoses</term>
<term>Mâle</term>
<term>Métastase lymphatique</term>
<term>Thrombophlébite</term>
<term>Vieillissement</term>
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<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>
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<Title>Zeitschrift fur Lymphologie. Journal of lymphology</Title>
<ISOAbbreviation>Z Lymphol</ISOAbbreviation>
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<ArticleTitle>[Primary lymphedema].</ArticleTitle>
<Pagination><MedlinePgn>21-8</MedlinePgn>
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<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>
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<MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName>
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<MeshHeading><DescriptorName UI="D004604" MajorTopicYN="N">Elephantiasis</DescriptorName>
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<MeshHeading><DescriptorName UI="D008207" MajorTopicYN="N">Lymphatic Metastasis</DescriptorName>
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