[Angiosarcoma in chronic lymphoedema: a case of Stewart-Treves syndrome].
Identifieur interne : 002D38 ( PubMed/Curation ); précédent : 002D37; suivant : 002D39[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. GennigensSource :
- Revue medicale de Liege [ 0370-629X ]
Descripteurs français
- KwdFr :
- Adulte d'âge moyen, Bras (anatomopathologie), Carcinomes (), Carcinomes (anatomopathologie), Femelle, Humains, Lymphadénectomie (effets indésirables), Lymphangiosarcome (), Lymphangiosarcome (diagnostic), Lymphangiosarcome (étiologie), Lymphoedème (), Lymphoedème (étiologie), Mastectomie (), Pronostic, Seconde tumeur primitive (), Seconde tumeur primitive (diagnostic), Seconde tumeur primitive (étiologie), Syndrome, Tumeurs cutanées (), Tumeurs cutanées (diagnostic), Tumeurs cutanées (étiologie), Tumeurs du sein (), Tumeurs du sein (anatomopathologie).
- MESH :
- anatomopathologie : Bras, Carcinomes, Tumeurs du sein.
- diagnostic : Lymphangiosarcome, Seconde tumeur primitive, Tumeurs cutanées.
- effets indésirables : Lymphadénectomie.
- étiologie : Lymphangiosarcome, Lymphoedème, Seconde tumeur primitive, Tumeurs cutanées.
- Adulte d'âge moyen, Carcinomes, Femelle, Humains, Lymphangiosarcome, Lymphoedème, Mastectomie, Pronostic, Seconde tumeur primitive, Syndrome, Tumeurs cutanées, Tumeurs du sein.
English descriptors
- KwdEn :
- Arm (pathology), Breast Neoplasms (pathology), Breast Neoplasms (surgery), Carcinoma (pathology), Carcinoma (surgery), Female, Humans, Lymph Node Excision (adverse effects), Lymphangiosarcoma (diagnosis), Lymphangiosarcoma (etiology), Lymphangiosarcoma (therapy), Lymphedema (complications), Lymphedema (etiology), Mastectomy (methods), Middle Aged, Neoplasms, Second Primary (diagnosis), Neoplasms, Second Primary (etiology), Neoplasms, Second Primary (therapy), Prognosis, Skin Neoplasms (diagnosis), Skin Neoplasms (etiology), Skin Neoplasms (therapy), Syndrome.
- MESH :
- adverse effects : Lymph Node Excision.
- complications : Lymphedema.
- diagnosis : Lymphangiosarcoma, Neoplasms, Second Primary, Skin Neoplasms.
- etiology : Lymphangiosarcoma, Lymphedema, Neoplasms, Second Primary, Skin Neoplasms.
- methods : Mastectomy.
- pathology : Arm, Breast Neoplasms, Carcinoma.
- surgery : Breast Neoplasms, Carcinoma.
- therapy : Lymphangiosarcoma, Neoplasms, Second Primary, Skin Neoplasms.
- Female, Humans, Middle Aged, Prognosis, Syndrome.
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:19777923Le document en format XML
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<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>
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<term>Neoplasms, Second Primary (etiology)</term>
<term>Neoplasms, Second Primary (therapy)</term>
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<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>
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<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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<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Lymph Node Excision</term>
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<term>Carcinomes</term>
<term>Tumeurs du sein</term>
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<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>
</keywords>
<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Lymphadénectomie</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphangiosarcoma</term>
<term>Lymphedema</term>
<term>Neoplasms, Second Primary</term>
<term>Skin Neoplasms</term>
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<term>Seconde tumeur primitive</term>
<term>Tumeurs cutanées</term>
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<term>Humans</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>
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<ArticleTitle>[Angiosarcoma in chronic lymphoedema: a case of Stewart-Treves syndrome].</ArticleTitle>
<Pagination><MedlinePgn>409-13</MedlinePgn>
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<Abstract><AbstractText>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.</AbstractText>
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