Lymphangiosarcoma in chronic lymphoedema. Stewart-Treves syndrome.
Identifieur interne : 004626 ( PubMed/Checkpoint ); précédent : 004625; suivant : 004627Lymphangiosarcoma in chronic lymphoedema. Stewart-Treves syndrome.
Auteurs : A C Aygit [Turquie] ; A M Yildirim ; S. DervisogluSource :
- Journal of hand surgery (Edinburgh, Scotland) [ 0266-7681 ] ; 1999.
Descripteurs français
- KwdFr :
- Adulte d'âge moyen, Amputation chirurgicale, Bras (), Bras (anatomopathologie), Femelle, Humains, Immunohistochimie, Lymphangiosarcome (), Lymphangiosarcome (secondaire), Lymphoedème (), Maladie chronique, Mastectomie radicale, Syndrome, Tumeurs cutanées (), Tumeurs cutanées (secondaire), Tumeurs du sein (), Tumeurs du sein (anatomopathologie).
- MESH :
- anatomopathologie : Bras, Tumeurs du sein.
- secondaire : Lymphangiosarcome, Tumeurs cutanées.
- Adulte d'âge moyen, Amputation chirurgicale, Bras, Femelle, Humains, Immunohistochimie, Lymphangiosarcome, Lymphoedème, Maladie chronique, Mastectomie radicale, Syndrome, Tumeurs cutanées, Tumeurs du sein.
English descriptors
- KwdEn :
- Amputation, Arm (pathology), Arm (surgery), Breast Neoplasms (pathology), Breast Neoplasms (surgery), Chronic Disease, Female, Humans, Immunohistochemistry, Lymphangiosarcoma (secondary), Lymphangiosarcoma (surgery), Lymphedema (complications), Mastectomy, Radical, Middle Aged, Skin Neoplasms (secondary), Skin Neoplasms (surgery), Syndrome.
- MESH :
- complications : Lymphedema.
- pathology : Arm, Breast Neoplasms.
- secondary : Lymphangiosarcoma, Skin Neoplasms.
- surgery : Arm, Breast Neoplasms, Lymphangiosarcoma, Skin Neoplasms.
- Amputation, Chronic Disease, Female, Humans, Immunohistochemistry, Mastectomy, Radical, Middle Aged, Syndrome.
Abstract
A case of post-mastectomy lymphangiosarcoma is reported. Lymphangiosarcoma is an extremely rare but highly lethal complication of chronic lymphoedema. Our patient was treated by amputation and died 6 months later. Treatment of post-mastectomy lymphangiosarcoma is still unsatisfactory. Early recognition and radical ablative surgery seem to provide best chance for survival.
DOI: 10.1054/jhsb.1998.0049
PubMed: 10190629
Affiliations:
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pubmed:10190629Le document en format XML
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<term>Breast Neoplasms (surgery)</term>
<term>Chronic Disease</term>
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<term>Immunohistochemistry</term>
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<term>Lymphedema (complications)</term>
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<term>Femelle</term>
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<term>Mastectomie radicale</term>
<term>Syndrome</term>
<term>Tumeurs cutanées ()</term>
<term>Tumeurs cutanées (secondaire)</term>
<term>Tumeurs du sein ()</term>
<term>Tumeurs du sein (anatomopathologie)</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Bras</term>
<term>Tumeurs du sein</term>
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<term>Amputation chirurgicale</term>
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<term>Humains</term>
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<term>Maladie chronique</term>
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<front><div type="abstract" xml:lang="en">A case of post-mastectomy lymphangiosarcoma is reported. Lymphangiosarcoma is an extremely rare but highly lethal complication of chronic lymphoedema. Our patient was treated by amputation and died 6 months later. Treatment of post-mastectomy lymphangiosarcoma is still unsatisfactory. Early recognition and radical ablative surgery seem to provide best chance for survival.</div>
</front>
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<Abstract><AbstractText>A case of post-mastectomy lymphangiosarcoma is reported. Lymphangiosarcoma is an extremely rare but highly lethal complication of chronic lymphoedema. Our patient was treated by amputation and died 6 months later. Treatment of post-mastectomy lymphangiosarcoma is still unsatisfactory. Early recognition and radical ablative surgery seem to provide best chance for survival.</AbstractText>
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