Lymphedema-induced lymphangiosarcoma
Identifieur interne : 00C570 ( Main/Exploration ); précédent : 00C569; suivant : 00C571Lymphedema-induced lymphangiosarcoma
Auteurs : Arieke J. Janse [Pays-Bas] ; Frits Van Coevorden [Pays-Bas] ; Hans Peterse [Pays-Bas] ; Ronald B. Keus [Pays-Bas] ; Johannes A. Van Dongen [Pays-Bas]Source :
- European Journal of Surgical Oncology [ 0748-7983 ] ; 1995.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphangiosarcome.
- effets indésirables : Association thérapeutique.
- étiologie : Lymphangiosarcome, Lymphoedème.
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Aged, Breast Neoplasms (complications), Breast Neoplasms (therapy), Combined Modality Therapy (adverse effects), Complication, Female, Human, Humans, Lymphangiosarcoma, Lymphangiosarcoma (diagnosis), Lymphangiosarcoma (etiology), Lymphangiosarcoma (therapy), Lymphedema, Lymphedema (complications), Lymphedema (congenital), Lymphedema (etiology), Male, Middle Aged, Stewart-Treves syndrome, angiosarcoma, breast carcinoma, lymphangiosarcoma, lymphedema.
- MESH :
- adverse effects : Combined Modality Therapy.
- complications : Breast Neoplasms, Lymphedema.
- congenital : Lymphedema.
- diagnosis : Lymphangiosarcoma.
- etiology : Lymphangiosarcoma, Lymphedema.
- therapy : Breast Neoplasms, Lymphangiosarcoma.
- Aged, Female, Humans, Male, Middle Aged.
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.
Url:
DOI: 10.1016/S0748-7983(95)90270-8
Affiliations:
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Le document en format XML
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<term>Breast Neoplasms (complications)</term>
<term>Breast Neoplasms (therapy)</term>
<term>Combined Modality Therapy (adverse effects)</term>
<term>Complication</term>
<term>Female</term>
<term>Human</term>
<term>Humans</term>
<term>Lymphangiosarcoma</term>
<term>Lymphangiosarcoma (diagnosis)</term>
<term>Lymphangiosarcoma (etiology)</term>
<term>Lymphangiosarcoma (therapy)</term>
<term>Lymphedema</term>
<term>Lymphedema (complications)</term>
<term>Lymphedema (congenital)</term>
<term>Lymphedema (etiology)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Stewart-Treves syndrome</term>
<term>angiosarcoma</term>
<term>breast carcinoma</term>
<term>lymphangiosarcoma</term>
<term>lymphedema</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Association thérapeutique (effets indésirables)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphangiosarcome ()</term>
<term>Lymphangiosarcome (diagnostic)</term>
<term>Lymphangiosarcome (étiologie)</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (étiologie)</term>
<term>Mâle</term>
<term>Sujet âgé</term>
<term>Tumeurs du sein ()</term>
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<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Combined Modality Therapy</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Breast Neoplasms</term>
<term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphangiosarcoma</term>
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<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Association thérapeutique</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphangiosarcoma</term>
<term>Lymphedema</term>
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<term>Lymphangiosarcoma</term>
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<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Lymphangiosarcome</term>
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<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
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<term>Femelle</term>
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<term>Humains</term>
<term>Lymphangiosarcome</term>
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<front><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>
</front>
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<name sortKey="Coevorden, Frits Van" sort="Coevorden, Frits Van" uniqKey="Coevorden F" first="Frits Van" last="Coevorden">Frits Van Coevorden</name>
<name sortKey="Dongen, Johannes A Van" sort="Dongen, Johannes A Van" uniqKey="Dongen J" first="Johannes A. Van" last="Dongen">Johannes A. Van Dongen</name>
<name sortKey="Keus, Ronald B" sort="Keus, Ronald B" uniqKey="Keus R" first="Ronald B." last="Keus">Ronald B. Keus</name>
<name sortKey="Peterse, Hans" sort="Peterse, Hans" uniqKey="Peterse H" first="Hans" last="Peterse">Hans Peterse</name>
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