Angiosarcoma in a limb with arteriovenous fistulas and elephantiasis.
Identifieur interne : 014142 ( Main/Merge ); précédent : 014141; suivant : 014143Angiosarcoma in a limb with arteriovenous fistulas and elephantiasis.
Auteurs : G L Faggioli [Italie] ; F. Bertoni ; P. Bacchini ; A. Stella ; M. Gessaroli ; M. GargiuloSource :
- International angiology : a journal of the International Union of Angiology [ 0392-9590 ]
Descripteurs français
- KwdFr :
- Adolescent, Angiomatose (), Complications postopératoires (anatomopathologie), Endothélium vasculaire (anatomopathologie), Femelle, Fistule artérioveineuse (anatomopathologie), Humains, Hémangiosarcome (anatomopathologie), Ischémie (anatomopathologie), Jambe (), Lymphoedème (anatomopathologie), Tumeurs des tissus mous (), Tumeurs des tissus mous (anatomopathologie), Tumeurs primitives multiples (anatomopathologie).
- MESH :
English descriptors
- KwdEn :
- Adolescent, Angiomatosis (surgery), Arteriovenous Fistula (pathology), Endothelium, Vascular (pathology), Female, Hemangiosarcoma (pathology), Humans, Ischemia (pathology), Leg (blood supply), Lymphedema (pathology), Neoplasms, Multiple Primary (pathology), Postoperative Complications (pathology), Soft Tissue Neoplasms (pathology), Soft Tissue Neoplasms (surgery).
- MESH :
- blood supply : Leg.
- pathology : Arteriovenous Fistula, Endothelium, Vascular, Hemangiosarcoma, Ischemia, Lymphedema, Neoplasms, Multiple Primary, Postoperative Complications, Soft Tissue Neoplasms.
- surgery : Angiomatosis, Soft Tissue Neoplasms.
- Adolescent, Female, Humans.
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
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pubmed:2592800Le document en format XML
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<author><name sortKey="Faggioli, G L" sort="Faggioli, G L" uniqKey="Faggioli G" first="G L" last="Faggioli">G L Faggioli</name>
<affiliation wicri:level="1"><nlm:affiliation>Chair of Vascular Surgery, University of Bologna, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Chair of Vascular Surgery, University of Bologna</wicri:regionArea>
<wicri:noRegion>University of Bologna</wicri:noRegion>
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<author><name sortKey="Bertoni, F" sort="Bertoni, F" uniqKey="Bertoni F" first="F" last="Bertoni">F. Bertoni</name>
</author>
<author><name sortKey="Bacchini, P" sort="Bacchini, P" uniqKey="Bacchini P" first="P" last="Bacchini">P. Bacchini</name>
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<author><name sortKey="Stella, A" sort="Stella, A" uniqKey="Stella A" first="A" last="Stella">A. Stella</name>
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<author><name sortKey="Gessaroli, M" sort="Gessaroli, M" uniqKey="Gessaroli M" first="M" last="Gessaroli">M. Gessaroli</name>
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<author><name sortKey="Gargiulo, M" sort="Gargiulo, M" uniqKey="Gargiulo M" first="M" last="Gargiulo">M. Gargiulo</name>
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<author><name sortKey="Faggioli, G L" sort="Faggioli, G L" uniqKey="Faggioli G" first="G L" last="Faggioli">G L Faggioli</name>
<affiliation wicri:level="1"><nlm:affiliation>Chair of Vascular Surgery, University of Bologna, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Chair of Vascular Surgery, University of Bologna</wicri:regionArea>
<wicri:noRegion>University of Bologna</wicri:noRegion>
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<author><name sortKey="Bertoni, F" sort="Bertoni, F" uniqKey="Bertoni F" first="F" last="Bertoni">F. Bertoni</name>
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<author><name sortKey="Bacchini, P" sort="Bacchini, P" uniqKey="Bacchini P" first="P" last="Bacchini">P. Bacchini</name>
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<author><name sortKey="Stella, A" sort="Stella, A" uniqKey="Stella A" first="A" last="Stella">A. Stella</name>
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<author><name sortKey="Gessaroli, M" sort="Gessaroli, M" uniqKey="Gessaroli M" first="M" last="Gessaroli">M. Gessaroli</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><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>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Angiomatose ()</term>
<term>Complications postopératoires (anatomopathologie)</term>
<term>Endothélium vasculaire (anatomopathologie)</term>
<term>Femelle</term>
<term>Fistule artérioveineuse (anatomopathologie)</term>
<term>Humains</term>
<term>Hémangiosarcome (anatomopathologie)</term>
<term>Ischémie (anatomopathologie)</term>
<term>Jambe ()</term>
<term>Lymphoedème (anatomopathologie)</term>
<term>Tumeurs des tissus mous ()</term>
<term>Tumeurs des tissus mous (anatomopathologie)</term>
<term>Tumeurs primitives multiples (anatomopathologie)</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Complications postopératoires</term>
<term>Endothélium vasculaire</term>
<term>Fistule artérioveineuse</term>
<term>Hémangiosarcome</term>
<term>Ischémie</term>
<term>Lymphoedème</term>
<term>Tumeurs des tissus mous</term>
<term>Tumeurs primitives multiples</term>
</keywords>
<keywords scheme="MESH" qualifier="blood supply" xml:lang="en"><term>Leg</term>
</keywords>
<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>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Angiomatosis</term>
<term>Soft Tissue Neoplasms</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Female</term>
<term>Humans</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Angiomatose</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jambe</term>
<term>Tumeurs des tissus mous</term>
</keywords>
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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>
</front>
</TEI>
</record>
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