LymphedemaV1, Main, Exploration, bibRecord, 007E10

[Stewart-Treves syndrome].

Identifieur interne : 007E10 ( Main/Exploration ); précédent : 007E09; suivant : 007E11

[Stewart-Treves syndrome].

Auteurs : Miguel Echenique-Elizondo [Espagne] ; Ana Tuneu-Valls ; José Zubizarreta ; Carmen Lobo

Source :

Cirugia espanola [ 0009-739X ] ; 2005.

RBID : pubmed:16420866

Descripteurs français

KwdFr :
- Adulte, Adulte d'âge moyen, Femelle, Humains, Lymphangiosarcome (), Lymphangiosarcome (diagnostic), Mâle, Sujet âgé, Syndrome, Études de suivi.
MESH :
- diagnostic : Lymphangiosarcome.
- Adulte, Adulte d'âge moyen, Femelle, Humains, Lymphangiosarcome, Mâle, Sujet âgé, Syndrome, Études de suivi.

English descriptors

KwdEn :
- Adult, Aged, Female, Follow-Up Studies, Humans, Lymphangiosarcoma (diagnosis), Lymphangiosarcoma (therapy), Male, Middle Aged, Syndrome.
MESH :
- diagnosis : Lymphangiosarcoma.
- therapy : Lymphangiosarcoma.
- Adult, Aged, Female, Follow-Up Studies, Humans, Male, Middle Aged, Syndrome.

Abstract

Lymphangiosarcoma is an uncommon vascular tumor that usually develops in longstanding lymphedema. We gathered the cases of lymphangioma observed in a hospital and attempted to analyze their characteristics: age, sex, localization, treatment and follow-up data. We studied five cases: three cases of Stewart-Treves syndrome after mastectomy and radiotherapy and two cases that developed in patients with late-onset congenital lymphedema. There were four women and one man. Radical surgery was performed in four patients. The techniques employed were: above-knee amputation (one patient), hip disarticulation (one patient), scapulo-humeral disarticulation (two patients) and gemcitabine and radiotherapy in one patient with metastatic disease at diagnosis. Three patients died in the first 14 months of follow-up, while two are disease free after 46 and 86 months respectively. This study confirms the poor prognosis of patients with Steward-Treves syndrome.

PubMed: 16420866

Affiliations:

Espagne

Le document en format XML

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<affiliation wicri:level="1"><nlm:affiliation>Unidad Docente de Medicina, Facultad de Medicina, Universidad del País Vasco, San Sebastián, Guipúzcoa, Spain. gepecelm@sc.ehu.es</nlm:affiliation>
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<author><name sortKey="Tuneu Valls, Ana" sort="Tuneu Valls, Ana" uniqKey="Tuneu Valls A" first="Ana" last="Tuneu-Valls">Ana Tuneu-Valls</name>
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<author><name sortKey="Echenique Elizondo, Miguel" sort="Echenique Elizondo, Miguel" uniqKey="Echenique Elizondo M" first="Miguel" last="Echenique-Elizondo">Miguel Echenique-Elizondo</name>
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<author><name sortKey="Tuneu Valls, Ana" sort="Tuneu Valls, Ana" uniqKey="Tuneu Valls A" first="Ana" last="Tuneu-Valls">Ana Tuneu-Valls</name>
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<author><name sortKey="Zubizarreta, Jose" sort="Zubizarreta, Jose" uniqKey="Zubizarreta J" first="José" last="Zubizarreta">José Zubizarreta</name>
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<series><title level="j">Cirugia espanola</title>
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<term>Aged</term>
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<term>Humans</term>
<term>Lymphangiosarcoma (diagnosis)</term>
<term>Lymphangiosarcoma (therapy)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Syndrome</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphangiosarcome ()</term>
<term>Lymphangiosarcome (diagnostic)</term>
<term>Mâle</term>
<term>Sujet âgé</term>
<term>Syndrome</term>
<term>Études de suivi</term>
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<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphangiosarcome</term>
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<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Lymphangiosarcoma</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
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<term>Lymphangiosarcome</term>
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<term>Syndrome</term>
<term>Études de suivi</term>
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<front><div type="abstract" xml:lang="en">Lymphangiosarcoma is an uncommon vascular tumor that usually develops in longstanding lymphedema. We gathered the cases of lymphangioma observed in a hospital and attempted to analyze their characteristics: age, sex, localization, treatment and follow-up data. We studied five cases: three cases of Stewart-Treves syndrome after mastectomy and radiotherapy and two cases that developed in patients with late-onset congenital lymphedema. There were four women and one man. Radical surgery was performed in four patients. The techniques employed were: above-knee amputation (one patient), hip disarticulation (one patient), scapulo-humeral disarticulation (two patients) and gemcitabine and radiotherapy in one patient with metastatic disease at diagnosis. Three patients died in the first 14 months of follow-up, while two are disease free after 46 and 86 months respectively. This study confirms the poor prognosis of patients with Steward-Treves syndrome.</div>
</front>
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<tree><noCountry><name sortKey="Lobo, Carmen" sort="Lobo, Carmen" uniqKey="Lobo C" first="Carmen" last="Lobo">Carmen Lobo</name>
<name sortKey="Tuneu Valls, Ana" sort="Tuneu Valls, Ana" uniqKey="Tuneu Valls A" first="Ana" last="Tuneu-Valls">Ana Tuneu-Valls</name>
<name sortKey="Zubizarreta, Jose" sort="Zubizarreta, Jose" uniqKey="Zubizarreta J" first="José" last="Zubizarreta">José Zubizarreta</name>
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<country name="Espagne"><noRegion><name sortKey="Echenique Elizondo, Miguel" sort="Echenique Elizondo, Miguel" uniqKey="Echenique Elizondo M" first="Miguel" last="Echenique-Elizondo">Miguel Echenique-Elizondo</name>
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Serveur d'exploration sur le lymphœdème

[Stewart-Treves syndrome].

[Stewart-Treves syndrome].

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

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

	Serveur d'exploration sur le lymphœdème
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