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[Angiosarcoma in chronic lymphoedema: a case of Stewart-Treves syndrome].

Identifieur interne : 003631 ( Ncbi/Curation ); précédent : 003630; suivant : 003632

[Angiosarcoma in chronic lymphoedema: a case of Stewart-Treves syndrome].

Auteurs : E. Gonne [Belgique] ; J. Collignon ; W. Kurth ; A. Thiry ; F. Henry ; G. Jerusalem ; C. Gennigens

Source :

RBID : pubmed:19777923

Descripteurs français

English descriptors

Abstract

The Stewart-Treves Syndrome is defined as an angiosarcoma (very aggressive malignant tumor originating from endothelial cells) appearing in a specific clinical setting. This tumor develops in patients suffering from chronic lymphedema of the upper limb following mastectomy and axillary lymph node dissection for breast cancer. The diagnosis relies on medical history, clinical examination and a histological assesment (biopsy or resection). This syndrome represents a rare clinical entity. Unfortunately, the prognosis is poor. A large surgical resection is the treatment of choice if the patient is a candidate for a surgical resection with a curative intent Radiotherapy is sometimes used as a palliative local treatment. Chemotherapy is only used in more advanced cases, not curable by surgery alone.

PubMed: 19777923

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pubmed:19777923

Le document en format XML

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<title xml:lang="en">[Angiosarcoma in chronic lymphoedema: a case of Stewart-Treves syndrome].</title>
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<name sortKey="Gonne, E" sort="Gonne, E" uniqKey="Gonne E" first="E" last="Gonne">E. Gonne</name>
<affiliation wicri:level="1">
<nlm:affiliation>Université de Liège, Belgique.</nlm:affiliation>
<country xml:lang="fr">Belgique</country>
<wicri:regionArea>Université de Liège</wicri:regionArea>
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<author>
<name sortKey="Collignon, J" sort="Collignon, J" uniqKey="Collignon J" first="J" last="Collignon">J. Collignon</name>
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<name sortKey="Kurth, W" sort="Kurth, W" uniqKey="Kurth W" first="W" last="Kurth">W. Kurth</name>
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<name sortKey="Thiry, A" sort="Thiry, A" uniqKey="Thiry A" first="A" last="Thiry">A. Thiry</name>
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<name sortKey="Henry, F" sort="Henry, F" uniqKey="Henry F" first="F" last="Henry">F. Henry</name>
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<name sortKey="Jerusalem, G" sort="Jerusalem, G" uniqKey="Jerusalem G" first="G" last="Jerusalem">G. Jerusalem</name>
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<name sortKey="Gennigens, C" sort="Gennigens, C" uniqKey="Gennigens C" first="C" last="Gennigens">C. Gennigens</name>
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<name sortKey="Henry, F" sort="Henry, F" uniqKey="Henry F" first="F" last="Henry">F. Henry</name>
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<name sortKey="Gennigens, C" sort="Gennigens, C" uniqKey="Gennigens C" first="C" last="Gennigens">C. Gennigens</name>
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<title level="j">Revue medicale de Liege</title>
<idno type="ISSN">0370-629X</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Arm (pathology)</term>
<term>Breast Neoplasms (pathology)</term>
<term>Breast Neoplasms (surgery)</term>
<term>Carcinoma (pathology)</term>
<term>Carcinoma (surgery)</term>
<term>Female</term>
<term>Humans</term>
<term>Lymph Node Excision (adverse effects)</term>
<term>Lymphangiosarcoma (diagnosis)</term>
<term>Lymphangiosarcoma (etiology)</term>
<term>Lymphangiosarcoma (therapy)</term>
<term>Lymphedema (complications)</term>
<term>Lymphedema (etiology)</term>
<term>Mastectomy (methods)</term>
<term>Middle Aged</term>
<term>Neoplasms, Second Primary (diagnosis)</term>
<term>Neoplasms, Second Primary (etiology)</term>
<term>Neoplasms, Second Primary (therapy)</term>
<term>Prognosis</term>
<term>Skin Neoplasms (diagnosis)</term>
<term>Skin Neoplasms (etiology)</term>
<term>Skin Neoplasms (therapy)</term>
<term>Syndrome</term>
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<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Bras (anatomopathologie)</term>
<term>Carcinomes ()</term>
<term>Carcinomes (anatomopathologie)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphadénectomie (effets indésirables)</term>
<term>Lymphangiosarcome ()</term>
<term>Lymphangiosarcome (diagnostic)</term>
<term>Lymphangiosarcome (étiologie)</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (étiologie)</term>
<term>Mastectomie ()</term>
<term>Pronostic</term>
<term>Seconde tumeur primitive ()</term>
<term>Seconde tumeur primitive (diagnostic)</term>
<term>Seconde tumeur primitive (étiologie)</term>
<term>Syndrome</term>
<term>Tumeurs cutanées ()</term>
<term>Tumeurs cutanées (diagnostic)</term>
<term>Tumeurs cutanées (étiologie)</term>
<term>Tumeurs du sein ()</term>
<term>Tumeurs du sein (anatomopathologie)</term>
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<term>Lymph Node Excision</term>
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<term>Bras</term>
<term>Carcinomes</term>
<term>Tumeurs du sein</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Lymphangiosarcoma</term>
<term>Neoplasms, Second Primary</term>
<term>Skin Neoplasms</term>
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<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr">
<term>Lymphangiosarcome</term>
<term>Seconde tumeur primitive</term>
<term>Tumeurs cutanées</term>
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<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr">
<term>Lymphadénectomie</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en">
<term>Lymphangiosarcoma</term>
<term>Lymphedema</term>
<term>Neoplasms, Second Primary</term>
<term>Skin Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Mastectomy</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Arm</term>
<term>Breast Neoplasms</term>
<term>Carcinoma</term>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en">
<term>Breast Neoplasms</term>
<term>Carcinoma</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en">
<term>Lymphangiosarcoma</term>
<term>Neoplasms, Second Primary</term>
<term>Skin Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr">
<term>Lymphangiosarcome</term>
<term>Lymphoedème</term>
<term>Seconde tumeur primitive</term>
<term>Tumeurs cutanées</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Prognosis</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Carcinomes</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphangiosarcome</term>
<term>Lymphoedème</term>
<term>Mastectomie</term>
<term>Pronostic</term>
<term>Seconde tumeur primitive</term>
<term>Syndrome</term>
<term>Tumeurs cutanées</term>
<term>Tumeurs du sein</term>
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<front>
<div type="abstract" xml:lang="en">The Stewart-Treves Syndrome is defined as an angiosarcoma (very aggressive malignant tumor originating from endothelial cells) appearing in a specific clinical setting. This tumor develops in patients suffering from chronic lymphedema of the upper limb following mastectomy and axillary lymph node dissection for breast cancer. The diagnosis relies on medical history, clinical examination and a histological assesment (biopsy or resection). This syndrome represents a rare clinical entity. Unfortunately, the prognosis is poor. A large surgical resection is the treatment of choice if the patient is a candidate for a surgical resection with a curative intent Radiotherapy is sometimes used as a palliative local treatment. Chemotherapy is only used in more advanced cases, not curable by surgery alone.</div>
</front>
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