Stewart Treves Syndrome*
Identifieur interne : 001816 ( Main/Exploration ); précédent : 001815; suivant : 001817Stewart Treves Syndrome*
Auteurs : Elisangela Samartin Pegas Pereira [Brésil] ; Elisa Trino De Moraes [Brésil] ; Daniela Melo Siqueira [Brésil] ; Marcel Alex Soares Dos Santos [Brésil]Source :
- Anais Brasileiros de Dermatologia [ 0365-0596 ] ; 2015.
Descripteurs français
- KwdFr :
- Amputation chirurgicale, Biopsie, Bras, Femelle, Humains, Hémangiosarcome (), Hémangiosarcome (anatomopathologie), Hémangiosarcome (étiologie), Lymphangiosarcome (), Lymphangiosarcome (anatomopathologie), Lymphangiosarcome (étiologie), Lymphoedème (), Lymphoedème (anatomopathologie), Lymphoedème (étiologie), Mastectomie, Récidive tumorale locale, Sujet âgé, Tumeurs cutanées (), Tumeurs cutanées (anatomopathologie), Tumeurs cutanées (étiologie).
- MESH :
- anatomopathologie : Hémangiosarcome, Lymphangiosarcome, Lymphoedème, Tumeurs cutanées.
- étiologie : Hémangiosarcome, Lymphangiosarcome, Lymphoedème, Tumeurs cutanées.
- Amputation chirurgicale, Biopsie, Bras, Femelle, Humains, Hémangiosarcome, Lymphangiosarcome, Lymphoedème, Mastectomie, Récidive tumorale locale, Sujet âgé, Tumeurs cutanées.
English descriptors
- KwdEn :
- Aged, Amputation, Arm, Biopsy, Female, Hemangiosarcoma (etiology), Hemangiosarcoma (pathology), Hemangiosarcoma (surgery), Humans, Lymphangiosarcoma (etiology), Lymphangiosarcoma (pathology), Lymphangiosarcoma (surgery), Lymphedema (etiology), Lymphedema (pathology), Lymphedema (surgery), Mastectomy, Neoplasm Recurrence, Local, Skin Neoplasms (etiology), Skin Neoplasms (pathology), Skin Neoplasms (surgery).
- MESH :
- etiology : Hemangiosarcoma, Lymphangiosarcoma, Lymphedema, Skin Neoplasms.
- pathology : Hemangiosarcoma, Lymphangiosarcoma, Lymphedema, Skin Neoplasms.
- surgery : Hemangiosarcoma, Lymphangiosarcoma, Lymphedema, Skin Neoplasms.
- Aged, Amputation, Arm, Biopsy, Female, Humans, Mastectomy, Neoplasm Recurrence, Local.
Abstract
Stewart-Treves Syndrome is characterized by the presence of lymphangiosarcoma on limb extremities. Rare, it occurs in 0.5% of patients who have undergone radical mastectomy with axillary node dissection. The main cause is chronic lymphedema with endothelial and lymphatic differentiation, with no direct relationship to breast cancer. Seven years after a radical right-side mastectomy with lymph node dissection and adjuvant therapy, the patient developed a lesion on her right arm. The dermatological examination revealed an erythematous nodule with bleeding surface on chronic right forearm lymphedema. After the biopsy, a lymphangiosarcoma on chronic lymphedema was diagnosed. Infrequent, this syndrome is relevant because of its associated mortality. Early diagnosis is important to improve survival and reduce complications.
Url:
DOI: 10.1590/abd1806-4841.20153685
PubMed: 26312725
PubMed Central: 4540559
Affiliations:
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Le document en format XML
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<series><title level="j">Anais Brasileiros de Dermatologia</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Amputation</term>
<term>Arm</term>
<term>Biopsy</term>
<term>Female</term>
<term>Hemangiosarcoma (etiology)</term>
<term>Hemangiosarcoma (pathology)</term>
<term>Hemangiosarcoma (surgery)</term>
<term>Humans</term>
<term>Lymphangiosarcoma (etiology)</term>
<term>Lymphangiosarcoma (pathology)</term>
<term>Lymphangiosarcoma (surgery)</term>
<term>Lymphedema (etiology)</term>
<term>Lymphedema (pathology)</term>
<term>Lymphedema (surgery)</term>
<term>Mastectomy</term>
<term>Neoplasm Recurrence, Local</term>
<term>Skin Neoplasms (etiology)</term>
<term>Skin Neoplasms (pathology)</term>
<term>Skin Neoplasms (surgery)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Amputation chirurgicale</term>
<term>Biopsie</term>
<term>Bras</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hémangiosarcome ()</term>
<term>Hémangiosarcome (anatomopathologie)</term>
<term>Hémangiosarcome (étiologie)</term>
<term>Lymphangiosarcome ()</term>
<term>Lymphangiosarcome (anatomopathologie)</term>
<term>Lymphangiosarcome (étiologie)</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (anatomopathologie)</term>
<term>Lymphoedème (étiologie)</term>
<term>Mastectomie</term>
<term>Récidive tumorale locale</term>
<term>Sujet âgé</term>
<term>Tumeurs cutanées ()</term>
<term>Tumeurs cutanées (anatomopathologie)</term>
<term>Tumeurs cutanées (étiologie)</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Hémangiosarcome</term>
<term>Lymphangiosarcome</term>
<term>Lymphoedème</term>
<term>Tumeurs cutanées</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Hemangiosarcoma</term>
<term>Lymphangiosarcoma</term>
<term>Lymphedema</term>
<term>Skin Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Hemangiosarcoma</term>
<term>Lymphangiosarcoma</term>
<term>Lymphedema</term>
<term>Skin Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Hemangiosarcoma</term>
<term>Lymphangiosarcoma</term>
<term>Lymphedema</term>
<term>Skin Neoplasms</term>
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<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Hémangiosarcome</term>
<term>Lymphangiosarcome</term>
<term>Lymphoedème</term>
<term>Tumeurs cutanées</term>
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<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Amputation</term>
<term>Arm</term>
<term>Biopsy</term>
<term>Female</term>
<term>Humans</term>
<term>Mastectomy</term>
<term>Neoplasm Recurrence, Local</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Amputation chirurgicale</term>
<term>Biopsie</term>
<term>Bras</term>
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<term>Humains</term>
<term>Hémangiosarcome</term>
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<front><div type="abstract" xml:lang="en"><p>Stewart-Treves Syndrome is characterized by the presence of lymphangiosarcoma on limb
extremities. Rare, it occurs in 0.5% of patients who have undergone radical
mastectomy with axillary node dissection. The main cause is chronic lymphedema with
endothelial and lymphatic differentiation, with no direct relationship to breast
cancer. Seven years after a radical right-side mastectomy with lymph node dissection
and adjuvant therapy, the patient developed a lesion on her right arm. The
dermatological examination revealed an erythematous nodule with bleeding surface on
chronic right forearm lymphedema. After the biopsy, a lymphangiosarcoma on chronic
lymphedema was diagnosed. Infrequent, this syndrome is relevant because of its
associated mortality. Early diagnosis is important to improve survival and reduce
complications.</p>
</div>
</front>
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