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MRI of angiosarcoma associated with chronic lymphoedema: Stewart Treves syndrome.

Identifieur interne : 007202 ( Main/Exploration ); précédent : 007201; suivant : 007203

MRI of angiosarcoma associated with chronic lymphoedema: Stewart Treves syndrome.

Auteurs : S. Chopra [États-Unis] ; F. Ors ; D. Bergin

Source :

RBID : pubmed:18065640

Descripteurs français

English descriptors

Abstract

Cutaneous angiosarcoma is a rare complication of a chronic lymphedematous extremity (Stewart-Treves syndrome). Early recognition of these aggressive tumours is important, as they have a high incidence of local recurrence and metastasis. This report describes the MRI appearance of Stewart-Treves syndrome in a patient with a background of lumpectomy, axillary node dissection and radiotherapy for breast carcinoma. MRI revealed a lobulated cutaneous mass of intermediate signal on T(1) weighted imaging, and low signal on T(2) weighted imaging, with diffuse enhancement following contrast.

DOI: 10.1259/bjr/19441948
PubMed: 18065640


Affiliations:


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Le document en format XML

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<term>Adulte d'âge moyen</term>
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<term>Lymphadénectomie (effets indésirables)</term>
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<div type="abstract" xml:lang="en">Cutaneous angiosarcoma is a rare complication of a chronic lymphedematous extremity (Stewart-Treves syndrome). Early recognition of these aggressive tumours is important, as they have a high incidence of local recurrence and metastasis. This report describes the MRI appearance of Stewart-Treves syndrome in a patient with a background of lumpectomy, axillary node dissection and radiotherapy for breast carcinoma. MRI revealed a lobulated cutaneous mass of intermediate signal on T(1) weighted imaging, and low signal on T(2) weighted imaging, with diffuse enhancement following contrast.</div>
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