Spindle cell hemangioendothelioma in association with epithelioid hemangioendothelioma.
Identifieur interne : 00B453 ( Ncbi/Merge ); précédent : 00B452; suivant : 00B454Spindle cell hemangioendothelioma in association with epithelioid hemangioendothelioma.
Auteurs : B. Azadeh [Qatar] ; M F Attallah ; G C EjeckamSource :
- Cutis [ 0011-4162 ] ; 1994.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Hémangioendothéliome, Hémangioendothéliome épithélioïde, Hémangiosarcome, Maladies du pied, Tumeurs cutanées, Tumeurs primitives multiples.
- Adulte, Humains, Mâle.
English descriptors
- KwdEn :
- MESH :
Abstract
A forty-two-year-old man presented with a twelve-year history of a multilobular, firm, but nonulcerated tumor (6 by 4.5 cm) of the dorsum of the right foot. He had capillary telangiectasia of both ankles but no lymphedema. Results of tests for human immunodeficiency viruses I and II were nonreactive. The tumor showed a complex combination of features of spindle cell hemangioendothelioma, epithelioid hemangioendothelioma, and areas suggestive of a possible well-differentiated (lymph) angiosarcoma. The tumor was completely excised with minimal healthy margin. There was no evidence of local or distant lesion at one-year follow-up examination.
PubMed: 8187542
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pubmed:8187542Le document en format XML
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<author><name sortKey="Azadeh, B" sort="Azadeh, B" uniqKey="Azadeh B" first="B" last="Azadeh">B. Azadeh</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Laboratory Medicine and Pathology, Hamad General Hospital, Doha, Qatar.</nlm:affiliation>
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<author><name sortKey="Attallah, M F" sort="Attallah, M F" uniqKey="Attallah M" first="M F" last="Attallah">M F Attallah</name>
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<author><name sortKey="Ejeckam, G C" sort="Ejeckam, G C" uniqKey="Ejeckam G" first="G C" last="Ejeckam">G C Ejeckam</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Foot Diseases (pathology)</term>
<term>Hemangioendothelioma (pathology)</term>
<term>Hemangioendothelioma, Epithelioid (pathology)</term>
<term>Hemangiosarcoma (pathology)</term>
<term>Humans</term>
<term>Male</term>
<term>Neoplasms, Multiple Primary (pathology)</term>
<term>Skin Neoplasms (pathology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term>
<term>Humains</term>
<term>Hémangioendothéliome (anatomopathologie)</term>
<term>Hémangioendothéliome épithélioïde (anatomopathologie)</term>
<term>Hémangiosarcome (anatomopathologie)</term>
<term>Maladies du pied (anatomopathologie)</term>
<term>Mâle</term>
<term>Tumeurs cutanées (anatomopathologie)</term>
<term>Tumeurs primitives multiples (anatomopathologie)</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Hémangioendothéliome</term>
<term>Hémangioendothéliome épithélioïde</term>
<term>Hémangiosarcome</term>
<term>Maladies du pied</term>
<term>Tumeurs cutanées</term>
<term>Tumeurs primitives multiples</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Foot Diseases</term>
<term>Hemangioendothelioma</term>
<term>Hemangioendothelioma, Epithelioid</term>
<term>Hemangiosarcoma</term>
<term>Neoplasms, Multiple Primary</term>
<term>Skin Neoplasms</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Humans</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte</term>
<term>Humains</term>
<term>Mâle</term>
</keywords>
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<front><div type="abstract" xml:lang="en">A forty-two-year-old man presented with a twelve-year history of a multilobular, firm, but nonulcerated tumor (6 by 4.5 cm) of the dorsum of the right foot. He had capillary telangiectasia of both ankles but no lymphedema. Results of tests for human immunodeficiency viruses I and II were nonreactive. The tumor showed a complex combination of features of spindle cell hemangioendothelioma, epithelioid hemangioendothelioma, and areas suggestive of a possible well-differentiated (lymph) angiosarcoma. The tumor was completely excised with minimal healthy margin. There was no evidence of local or distant lesion at one-year follow-up examination.</div>
</front>
</TEI>
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<DateRevised><Year>2013</Year>
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<JournalIssue CitedMedium="Print"><Volume>53</Volume>
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<Title>Cutis</Title>
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<ArticleTitle>Spindle cell hemangioendothelioma in association with epithelioid hemangioendothelioma.</ArticleTitle>
<Pagination><MedlinePgn>134-6</MedlinePgn>
</Pagination>
<Abstract><AbstractText>A forty-two-year-old man presented with a twelve-year history of a multilobular, firm, but nonulcerated tumor (6 by 4.5 cm) of the dorsum of the right foot. He had capillary telangiectasia of both ankles but no lymphedema. Results of tests for human immunodeficiency viruses I and II were nonreactive. The tumor showed a complex combination of features of spindle cell hemangioendothelioma, epithelioid hemangioendothelioma, and areas suggestive of a possible well-differentiated (lymph) angiosarcoma. The tumor was completely excised with minimal healthy margin. There was no evidence of local or distant lesion at one-year follow-up examination.</AbstractText>
</Abstract>
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