Serveur d'exploration sur le lymphœdème

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Lymphedema-induced lymphangiosarcoma

Identifieur interne : 00D069 ( Main/Merge ); précédent : 00D068; suivant : 00D070

Lymphedema-induced lymphangiosarcoma

Auteurs : A. J. Janse [Pays-Bas] ; F. Van Coevorden ; H. Peterse ; R. B. Keus ; J. A. Van Dongen

Source :

RBID : Pascal:95-0317196

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English descriptors

Abstract

A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed

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Pascal:95-0317196

Le document en format XML

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<title xml:lang="en" level="a">Lymphedema-induced lymphangiosarcoma</title>
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<name sortKey="Janse, A J" sort="Janse, A J" uniqKey="Janse A" first="A. J." last="Janse">A. J. Janse</name>
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<s1>Netherlands cancer inst., dep. surgery</s1>
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<country>Pays-Bas</country>
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<name sortKey="Van Coevorden, F" sort="Van Coevorden, F" uniqKey="Van Coevorden F" first="F." last="Van Coevorden">F. Van Coevorden</name>
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<name sortKey="Peterse, H" sort="Peterse, H" uniqKey="Peterse H" first="H." last="Peterse">H. Peterse</name>
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<term>Lymphangiosarcome</term>
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<div type="abstract" xml:lang="en">A series of eight patients with chronic lymphedema-related lymphangiosarcoma is presented. All but one case showed a typical rapid progression and fatal outcome, as has been reported in other series. In one patient the lymphangiosarcoma developed on the chest wall, the axilla and the arm where persisting lymphedema and fibrosis occurred after bilateral mastectomy and bilateral postoperative radiotherapy. In this patient an asymptomatic course and slow locoregional progression of lesions was seen. The clinical picture, the etiological considerations and the therapeutic options of the lymphedema-induced lymphangiosarcoma with regard to the literature are discussed</div>
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{{Explor lien
   |wiki=    Wicri/Sante
   |area=    LymphedemaV1
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   |clé=     Pascal:95-0317196
   |texte=   Lymphedema-induced lymphangiosarcoma
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