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Angiosarcoma in a limb with arteriovenous fistulas and elephantiasis.

Identifieur interne : 005F72 ( PubMed/Corpus ); précédent : 005F71; suivant : 005F73

Angiosarcoma in a limb with arteriovenous fistulas and elephantiasis.

Auteurs : G L Faggioli ; F. Bertoni ; P. Bacchini ; A. Stella ; M. Gessaroli ; M. Gargiulo

Source :

RBID : pubmed:2592800

English descriptors

Abstract

Angiosarcoma is a rare malignant tumor of the soft tissues (less than 1% of sarcoma). It may affect various parenchymae (bones, liver, breast), the soft tissues or the skin. In the latter case it may be associated with lymphedema. Onset in the arm is typical with postmastectomy lymphedema (Stewart-Treves syndrome). The forms occurring in limbs with chronic lymphedema not associated with mastectomy are much rarer, with a total of 38 cases occurring in patients with an average age of 46.8 years and with lymphedema present for an average of 20 years. The survival rate for 5 years is 16.6%. The case observed by us had the characteristic onset of the malignant neoplasm on a pre-existing "angiomatosis lymphangiomatosis" pattern also featuring angiographycally detected arteriovenous fistula.

PubMed: 2592800

Links to Exploration step

pubmed:2592800

Le document en format XML

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<title xml:lang="en">Angiosarcoma in a limb with arteriovenous fistulas and elephantiasis.</title>
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<name sortKey="Faggioli, G L" sort="Faggioli, G L" uniqKey="Faggioli G" first="G L" last="Faggioli">G L Faggioli</name>
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<nlm:affiliation>Chair of Vascular Surgery, University of Bologna, Italy.</nlm:affiliation>
</affiliation>
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<name sortKey="Bertoni, F" sort="Bertoni, F" uniqKey="Bertoni F" first="F" last="Bertoni">F. Bertoni</name>
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<name sortKey="Bacchini, P" sort="Bacchini, P" uniqKey="Bacchini P" first="P" last="Bacchini">P. Bacchini</name>
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<name sortKey="Stella, A" sort="Stella, A" uniqKey="Stella A" first="A" last="Stella">A. Stella</name>
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<name sortKey="Gessaroli, M" sort="Gessaroli, M" uniqKey="Gessaroli M" first="M" last="Gessaroli">M. Gessaroli</name>
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<name sortKey="Gargiulo, M" sort="Gargiulo, M" uniqKey="Gargiulo M" first="M" last="Gargiulo">M. Gargiulo</name>
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<name sortKey="Bertoni, F" sort="Bertoni, F" uniqKey="Bertoni F" first="F" last="Bertoni">F. Bertoni</name>
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<name sortKey="Bacchini, P" sort="Bacchini, P" uniqKey="Bacchini P" first="P" last="Bacchini">P. Bacchini</name>
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<name sortKey="Stella, A" sort="Stella, A" uniqKey="Stella A" first="A" last="Stella">A. Stella</name>
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<term>Adolescent</term>
<term>Angiomatosis (surgery)</term>
<term>Arteriovenous Fistula (pathology)</term>
<term>Endothelium, Vascular (pathology)</term>
<term>Female</term>
<term>Hemangiosarcoma (pathology)</term>
<term>Humans</term>
<term>Ischemia (pathology)</term>
<term>Leg (blood supply)</term>
<term>Lymphedema (pathology)</term>
<term>Neoplasms, Multiple Primary (pathology)</term>
<term>Postoperative Complications (pathology)</term>
<term>Soft Tissue Neoplasms (pathology)</term>
<term>Soft Tissue Neoplasms (surgery)</term>
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<term>Leg</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Arteriovenous Fistula</term>
<term>Endothelium, Vascular</term>
<term>Hemangiosarcoma</term>
<term>Ischemia</term>
<term>Lymphedema</term>
<term>Neoplasms, Multiple Primary</term>
<term>Postoperative Complications</term>
<term>Soft Tissue Neoplasms</term>
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<keywords scheme="MESH" qualifier="surgery" xml:lang="en">
<term>Angiomatosis</term>
<term>Soft Tissue Neoplasms</term>
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<keywords scheme="MESH" xml:lang="en">
<term>Adolescent</term>
<term>Female</term>
<term>Humans</term>
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<front>
<div type="abstract" xml:lang="en">Angiosarcoma is a rare malignant tumor of the soft tissues (less than 1% of sarcoma). It may affect various parenchymae (bones, liver, breast), the soft tissues or the skin. In the latter case it may be associated with lymphedema. Onset in the arm is typical with postmastectomy lymphedema (Stewart-Treves syndrome). The forms occurring in limbs with chronic lymphedema not associated with mastectomy are much rarer, with a total of 38 cases occurring in patients with an average age of 46.8 years and with lymphedema present for an average of 20 years. The survival rate for 5 years is 16.6%. The case observed by us had the characteristic onset of the malignant neoplasm on a pre-existing "angiomatosis lymphangiomatosis" pattern also featuring angiographycally detected arteriovenous fistula.</div>
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<Title>International angiology : a journal of the International Union of Angiology</Title>
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<ArticleTitle>Angiosarcoma in a limb with arteriovenous fistulas and elephantiasis.</ArticleTitle>
<Pagination>
<MedlinePgn>161-70</MedlinePgn>
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<AbstractText>Angiosarcoma is a rare malignant tumor of the soft tissues (less than 1% of sarcoma). It may affect various parenchymae (bones, liver, breast), the soft tissues or the skin. In the latter case it may be associated with lymphedema. Onset in the arm is typical with postmastectomy lymphedema (Stewart-Treves syndrome). The forms occurring in limbs with chronic lymphedema not associated with mastectomy are much rarer, with a total of 38 cases occurring in patients with an average age of 46.8 years and with lymphedema present for an average of 20 years. The survival rate for 5 years is 16.6%. The case observed by us had the characteristic onset of the malignant neoplasm on a pre-existing "angiomatosis lymphangiomatosis" pattern also featuring angiographycally detected arteriovenous fistula.</AbstractText>
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