Stewart-Treves syndrome as a rare complication of a hereditary lymphedema
Identifieur interne : 000329 ( PascalFrancis/Curation ); précédent : 000328; suivant : 000330Stewart-Treves syndrome as a rare complication of a hereditary lymphedema
Auteurs : H. R. Dürr [Allemagne] ; C. Pellengahr [Allemagne] ; A. Nerlich [Allemagne] ; A. Baur [Allemagne] ; M. Maier [Allemagne] ; V. Jansson [Allemagne]Source :
- VASA [ 0301-1526 ] ; 2004.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Lymphangiosarcoma (LAS) may occur as a rare complication of primary lymphedema. A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.
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Pascal:04-0365449Le document en format XML
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<front><div type="abstract" xml:lang="en">Lymphangiosarcoma (LAS) may occur as a rare complication of primary lymphedema. A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.</div>
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