[Lymphangiosarcoma following mastectomy: review of the literature apropos of 2 recent cases of Stewart-Treves syndrome].
Identifieur interne : 006067 ( PubMed/Curation ); précédent : 006066; suivant : 006068[Lymphangiosarcoma following mastectomy: review of the literature apropos of 2 recent cases of Stewart-Treves syndrome].
Auteurs : J O Defraigne ; B. Detroz ; J. DuboisSource :
- Acta chirurgica Belgica [ 0001-5458 ]
Descripteurs français
- KwdFr :
- Bras, Désarticulation, Femelle, Humains, Lymphoedème (), Lymphoedème (étiologie), Lymphome malin non hodgkinien (), Lymphome malin non hodgkinien (traitement médicamenteux), Lymphome malin non hodgkinien (étiologie), Mastectomie radicale (effets indésirables), Protocoles de polychimiothérapie antinéoplasique (usage thérapeutique), Sujet âgé, Syndrome, Tumeurs des tissus mous (), Tumeurs des tissus mous (traitement médicamenteux), Tumeurs des tissus mous (étiologie).
- MESH :
- effets indésirables : Mastectomie radicale.
- traitement médicamenteux : Lymphome malin non hodgkinien, Tumeurs des tissus mous.
- usage thérapeutique : Protocoles de polychimiothérapie antinéoplasique.
- étiologie : Lymphoedème, Lymphome malin non hodgkinien, Tumeurs des tissus mous.
- Bras, Désarticulation, Femelle, Humains, Lymphoedème, Lymphome malin non hodgkinien, Sujet âgé, Syndrome, Tumeurs des tissus mous.
English descriptors
- KwdEn :
- Aged, Antineoplastic Combined Chemotherapy Protocols (therapeutic use), Arm, Disarticulation, Female, Humans, Lymphedema (complications), Lymphedema (etiology), Lymphoma, Non-Hodgkin (drug therapy), Lymphoma, Non-Hodgkin (etiology), Lymphoma, Non-Hodgkin (surgery), Mastectomy, Radical (adverse effects), Soft Tissue Neoplasms (drug therapy), Soft Tissue Neoplasms (etiology), Soft Tissue Neoplasms (surgery), Syndrome.
- MESH :
- adverse effects : Mastectomy, Radical.
- complications : Lymphedema.
- drug therapy : Lymphoma, Non-Hodgkin, Soft Tissue Neoplasms.
- etiology : Lymphedema, Lymphoma, Non-Hodgkin, Soft Tissue Neoplasms.
- surgery : Lymphoma, Non-Hodgkin, Soft Tissue Neoplasms.
- therapeutic use : Antineoplastic Combined Chemotherapy Protocols.
- Aged, Arm, Disarticulation, Female, Humans, Syndrome.
Abstract
Two cases of lymphangiosarcomas which arose 4 and 14 years after a mastectomy are reported (Stewart-Treves syndrome). One of the patients was treated by shoulder disarticulation and the other by chemotherapy (using Melphalan, Cyclophosphamide and 5-fluorouracil). Disseminated metastases and deaths occurred 6 and 18 months after the onset of the lesion. Stewart-Treves syndrome occurs in approximately 0.07 to 0.45% of mastectomy. Prognosis is worse: survival at five year is fewer than 10%. Early diagnosis is mandatory. Surgical resection of the lesions and adjunctive chemotherapy seem the best treatment.
PubMed: 2655358
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J O Defraigne<affiliation><nlm:affiliation>Service de chirurgie cardio-vasculaire et digestive, Centre Hospitalier Universitaire de Liège, Sart-Tilman.</nlm:affiliation>
<wicri:noCountry code="subField">Sart-Tilman</wicri:noCountry>
</affiliation>
Le document en format XML
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<author><name sortKey="Detroz, B" sort="Detroz, B" uniqKey="Detroz B" first="B" last="Detroz">B. Detroz</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[Lymphangiosarcoma following mastectomy: review of the literature apropos of 2 recent cases of Stewart-Treves syndrome].</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Antineoplastic Combined Chemotherapy Protocols (therapeutic use)</term>
<term>Arm</term>
<term>Disarticulation</term>
<term>Female</term>
<term>Humans</term>
<term>Lymphedema (complications)</term>
<term>Lymphedema (etiology)</term>
<term>Lymphoma, Non-Hodgkin (drug therapy)</term>
<term>Lymphoma, Non-Hodgkin (etiology)</term>
<term>Lymphoma, Non-Hodgkin (surgery)</term>
<term>Mastectomy, Radical (adverse effects)</term>
<term>Soft Tissue Neoplasms (drug therapy)</term>
<term>Soft Tissue Neoplasms (etiology)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Bras</term>
<term>Désarticulation</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (étiologie)</term>
<term>Lymphome malin non hodgkinien ()</term>
<term>Lymphome malin non hodgkinien (traitement médicamenteux)</term>
<term>Lymphome malin non hodgkinien (étiologie)</term>
<term>Mastectomie radicale (effets indésirables)</term>
<term>Protocoles de polychimiothérapie antinéoplasique (usage thérapeutique)</term>
<term>Sujet âgé</term>
<term>Syndrome</term>
<term>Tumeurs des tissus mous ()</term>
<term>Tumeurs des tissus mous (traitement médicamenteux)</term>
<term>Tumeurs des tissus mous (étiologie)</term>
</keywords>
<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Mastectomy, Radical</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Lymphoma, Non-Hodgkin</term>
<term>Soft Tissue Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Mastectomie radicale</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphedema</term>
<term>Lymphoma, Non-Hodgkin</term>
<term>Soft Tissue Neoplasms</term>
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<keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Lymphoma, Non-Hodgkin</term>
<term>Soft Tissue Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="therapeutic use" xml:lang="en"><term>Antineoplastic Combined Chemotherapy Protocols</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr"><term>Lymphome malin non hodgkinien</term>
<term>Tumeurs des tissus mous</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Protocoles de polychimiothérapie antinéoplasique</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Lymphoedème</term>
<term>Lymphome malin non hodgkinien</term>
<term>Tumeurs des tissus mous</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Arm</term>
<term>Disarticulation</term>
<term>Female</term>
<term>Humans</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Bras</term>
<term>Désarticulation</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Lymphome malin non hodgkinien</term>
<term>Sujet âgé</term>
<term>Syndrome</term>
<term>Tumeurs des tissus mous</term>
</keywords>
</textClass>
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<front><div type="abstract" xml:lang="en">Two cases of lymphangiosarcomas which arose 4 and 14 years after a mastectomy are reported (Stewart-Treves syndrome). One of the patients was treated by shoulder disarticulation and the other by chemotherapy (using Melphalan, Cyclophosphamide and 5-fluorouracil). Disseminated metastases and deaths occurred 6 and 18 months after the onset of the lesion. Stewart-Treves syndrome occurs in approximately 0.07 to 0.45% of mastectomy. Prognosis is worse: survival at five year is fewer than 10%. Early diagnosis is mandatory. Surgical resection of the lesions and adjunctive chemotherapy seem the best treatment.</div>
</front>
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<Title>Acta chirurgica Belgica</Title>
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<ArticleTitle>[Lymphangiosarcoma following mastectomy: review of the literature apropos of 2 recent cases of Stewart-Treves syndrome].</ArticleTitle>
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<Abstract><AbstractText>Two cases of lymphangiosarcomas which arose 4 and 14 years after a mastectomy are reported (Stewart-Treves syndrome). One of the patients was treated by shoulder disarticulation and the other by chemotherapy (using Melphalan, Cyclophosphamide and 5-fluorouracil). Disseminated metastases and deaths occurred 6 and 18 months after the onset of the lesion. Stewart-Treves syndrome occurs in approximately 0.07 to 0.45% of mastectomy. Prognosis is worse: survival at five year is fewer than 10%. Early diagnosis is mandatory. Surgical resection of the lesions and adjunctive chemotherapy seem the best treatment.</AbstractText>
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