Papillary intralymphatic angioendothelioma of the thigh: A case report and review of the literature.
Identifieur interne : 003A63 ( Ncbi/Checkpoint ); précédent : 003A62; suivant : 003A64Papillary intralymphatic angioendothelioma of the thigh: A case report and review of the literature.
Auteurs : Katherine A. Ward [États-Unis] ; Phillip M. Ecker ; Rebekah R. White ; Tanya E. Melnik ; Evin H. Gulbahce ; Mark S. Wilke ; Omar P. SanguezaSource :
- Dermatology online journal [ 1087-2108 ] ; 2010.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Hémangiosarcome, Tumeurs cutanées.
- diagnostic : Hémangiosarcome, Tumeurs cutanées.
- Adulte d'âge moyen, Cuisse, Diagnostic différentiel, Femelle, Humains, Hémangiosarcome, Tumeurs cutanées.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Hemangiosarcoma, Skin Neoplasms.
- pathology : Hemangiosarcoma, Skin Neoplasms.
- surgery : Hemangiosarcoma, Skin Neoplasms.
- Diagnosis, Differential, Female, Humans, Middle Aged, Thigh.
Abstract
The term angiosarcoma, encompasses several neoplasms, all of which exhibit a malignant process derived from endothelial cells of the vessels. The most common form of angiosarcoma is highly aggressive, often fatal, and usually affects the head and neck region of elderly white men. Other low-grade forms of angiosarcoma, including papillary intralymphatic angioendothelioma, also known as Dabska tumor, are less invasive, affect a wider age range, and offer a better prognosis. There are several predisposing factors that increase the risk of angiosarcoma and include chronic lymphedema of the extremities, preexisting vascular lesions, and prior radiation, often as therapy for other malignancies. We report an unusual case of a very small, low-grade angiosarcoma on the thigh of an adult female with no known predisposing risk factors.
PubMed: 20409411
Affiliations:
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pubmed:20409411Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Papillary intralymphatic angioendothelioma of the thigh: A case report and review of the literature.</title>
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<term>Hemangiosarcoma (surgery)</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Skin Neoplasms (diagnosis)</term>
<term>Skin Neoplasms (pathology)</term>
<term>Skin Neoplasms (surgery)</term>
<term>Thigh</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Cuisse</term>
<term>Diagnostic différentiel</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hémangiosarcome ()</term>
<term>Hémangiosarcome (anatomopathologie)</term>
<term>Hémangiosarcome (diagnostic)</term>
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<term>Tumeurs cutanées (anatomopathologie)</term>
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<term>Skin Neoplasms</term>
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<term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
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<term>Cuisse</term>
<term>Diagnostic différentiel</term>
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<term>Humains</term>
<term>Hémangiosarcome</term>
<term>Tumeurs cutanées</term>
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<front><div type="abstract" xml:lang="en">The term angiosarcoma, encompasses several neoplasms, all of which exhibit a malignant process derived from endothelial cells of the vessels. The most common form of angiosarcoma is highly aggressive, often fatal, and usually affects the head and neck region of elderly white men. Other low-grade forms of angiosarcoma, including papillary intralymphatic angioendothelioma, also known as Dabska tumor, are less invasive, affect a wider age range, and offer a better prognosis. There are several predisposing factors that increase the risk of angiosarcoma and include chronic lymphedema of the extremities, preexisting vascular lesions, and prior radiation, often as therapy for other malignancies. We report an unusual case of a very small, low-grade angiosarcoma on the thigh of an adult female with no known predisposing risk factors.</div>
</front>
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<name sortKey="Sangueza, Omar P" sort="Sangueza, Omar P" uniqKey="Sangueza O" first="Omar P" last="Sangueza">Omar P. Sangueza</name>
<name sortKey="White, Rebekah R" sort="White, Rebekah R" uniqKey="White R" first="Rebekah R" last="White">Rebekah R. White</name>
<name sortKey="Wilke, Mark S" sort="Wilke, Mark S" uniqKey="Wilke M" first="Mark S" last="Wilke">Mark S. Wilke</name>
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<country name="États-Unis"><noRegion><name sortKey="Ward, Katherine A" sort="Ward, Katherine A" uniqKey="Ward K" first="Katherine A" last="Ward">Katherine A. Ward</name>
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