Le syndrome de Stewart-Treves compliquant un lymphœdème chronique idiopathique
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منابع مشابه
Le syndrome de Stewart-Treves compliquant un lymphœdème chronique idiopathique
Le syndrome de Stewart-Treves (SST) est une entité rare, correspondant à un angiosarcome cutané compliquant un lymphoedème chronique. Il est de mauvais pronostic. Stewart et Treves ont rapportés en 1948, les premiers cas d'angiosarcome secondaire à un traitement du cancer du sein. Ce terme s'est généralisé pour regrouper l'ensemble des cas de lymphangiosarcome sur lymphoedème d'origine congénit...
متن کاملSyndrome de Stewart-Treves: complication rare de lymphœdème chronique
Pan African Medical Journal. 2016; 24:196 doi:10.11604/pamj.2016.24.196.8540 This article is available online at: http://www.panafrican-med-journal.com/content/article/24/196/full/ © Sanaa Krich et al. The Pan African Medical Journal ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0)...
متن کاملSyndrome de Stewart Treves: une complication redoutable du lymphœdème
Stewart-treves syndrome (SST), also known as cutaneous angiosarcoma, is a rare and extremely serious complication of chronic lymphedema. Diagnosis is based on histology and immunohistochemistry. Treatment is primarily surgical. This syndrome occurs in 90% of cases after breast surgery. However, it can sometimes occur from other causes, as illustrated in our case study. The prognosis of Stewart-...
متن کاملStewart-Treves syndrome
Stewart-Treves syndrome is a rare cutaneous angiosarcoma with a poor prognosis. Physicians must be aware of this lethal syndrome, especially in patients who have been treated for breast cancer with radiation and lymph-node dissection (such as the case reported here). Patients who develop unexplained enlarging plaques of coalescing purple papules should have immediate biopsy for early diagnosis ...
متن کاملStewart Treves Syndrome*
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 n...
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ژورنال
عنوان ژورنال: Pan African Medical Journal
سال: 2014
ISSN: 1937-8688
DOI: 10.11604/pamj.2014.19.311.5636