Lymphangiosarcoma in chronic lymphedema. Reports of 3 cases and review of the literature.
Identifieur interne : 00F753 ( Main/Merge ); précédent : 00F752; suivant : 00F754Lymphangiosarcoma in chronic lymphedema. Reports of 3 cases and review of the literature.
Auteurs : I H Borel Rinkes ; A B De JongsteSource :
- Acta chirurgica Scandinavica [ 0001-5482 ] ; 1986.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Lymphangiosarcome, Peau.
- mortalité : Lymphangiosarcome.
- étiologie : Lymphangiosarcome.
- Adulte d'âge moyen, Bras, Cuisse, Femelle, Humains, Lymphoedème, Mastectomie, Pronostic, Soins palliatifs, Sujet âgé.
English descriptors
- KwdEn :
- MESH :
- complications : Lymphedema.
- etiology : Lymphangiosarcoma.
- mortality : Lymphangiosarcoma.
- pathology : Lymphangiosarcoma, Skin.
- Aged, Arm, Female, Humans, Mastectomy, Middle Aged, Palliative Care, Prognosis, Thigh.
Abstract
Lymphangiosarcoma is an extremely rare but highly lethal complication of chronic lymphedema. The classic clinical picture is described and three cases are presented. Current concepts of etiology, histopathology, treatment and prognosis are discussed. Since early diagnosis may be the key to longer survival, all patients with chronic lymphedema should undergo careful examination at regular intervals throughout their lives.
PubMed: 2424204
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pubmed:2424204Le document en format XML
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<author><name sortKey="De Jongste, A B" sort="De Jongste, A B" uniqKey="De Jongste A" first="A B" last="De Jongste">A B De Jongste</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Lymphangiosarcoma in chronic lymphedema. Reports of 3 cases and review of the literature.</title>
<author><name sortKey="Borel Rinkes, I H" sort="Borel Rinkes, I H" uniqKey="Borel Rinkes I" first="I H" last="Borel Rinkes">I H Borel Rinkes</name>
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<series><title level="j">Acta chirurgica Scandinavica</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Arm</term>
<term>Female</term>
<term>Humans</term>
<term>Lymphangiosarcoma (etiology)</term>
<term>Lymphangiosarcoma (mortality)</term>
<term>Lymphangiosarcoma (pathology)</term>
<term>Lymphedema (complications)</term>
<term>Mastectomy</term>
<term>Middle Aged</term>
<term>Palliative Care</term>
<term>Prognosis</term>
<term>Skin (pathology)</term>
<term>Thigh</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Bras</term>
<term>Cuisse</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphangiosarcome (anatomopathologie)</term>
<term>Lymphangiosarcome (mortalité)</term>
<term>Lymphangiosarcome (étiologie)</term>
<term>Lymphoedème ()</term>
<term>Mastectomie</term>
<term>Peau (anatomopathologie)</term>
<term>Pronostic</term>
<term>Soins palliatifs</term>
<term>Sujet âgé</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphangiosarcome</term>
<term>Peau</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphangiosarcoma</term>
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<keywords scheme="MESH" qualifier="mortality" xml:lang="en"><term>Lymphangiosarcoma</term>
</keywords>
<keywords scheme="MESH" qualifier="mortalité" xml:lang="fr"><term>Lymphangiosarcome</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphangiosarcoma</term>
<term>Skin</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Lymphangiosarcome</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Arm</term>
<term>Female</term>
<term>Humans</term>
<term>Mastectomy</term>
<term>Middle Aged</term>
<term>Palliative Care</term>
<term>Prognosis</term>
<term>Thigh</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Bras</term>
<term>Cuisse</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Mastectomie</term>
<term>Pronostic</term>
<term>Soins palliatifs</term>
<term>Sujet âgé</term>
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<front><div type="abstract" xml:lang="en">Lymphangiosarcoma is an extremely rare but highly lethal complication of chronic lymphedema. The classic clinical picture is described and three cases are presented. Current concepts of etiology, histopathology, treatment and prognosis are discussed. Since early diagnosis may be the key to longer survival, all patients with chronic lymphedema should undergo careful examination at regular intervals throughout their lives.</div>
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