Papillary intralymphatic angioendothelioma of the thigh: A case report and review of the literature.
Identifieur interne : 002773 ( PubMed/Checkpoint ); précédent : 002772; suivant : 002774Papillary 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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Melnik</name></author><author><name sortKey="Gulbahce, Evin H" sort="Gulbahce, Evin H" uniqKey="Gulbahce E" first="Evin H" last="Gulbahce">Evin H. Gulbahce</name></author><author><name sortKey="Wilke, Mark S" sort="Wilke, Mark S" uniqKey="Wilke M" first="Mark S" last="Wilke">Mark S. Wilke</name></author><author><name sortKey="Sangueza, Omar P" sort="Sangueza, Omar P" uniqKey="Sangueza O" first="Omar P" last="Sangueza">Omar P. 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Wilke</name></author><author><name sortKey="Sangueza, Omar P" sort="Sangueza, Omar P" uniqKey="Sangueza O" first="Omar P" last="Sangueza">Omar P. Sangueza</name></author></analytic><series><title level="j">Dermatology online journal</title><idno type="eISSN">1087-2108</idno><imprint><date when="2010" type="published">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Diagnosis, Differential</term><term>Female</term><term>Hemangiosarcoma (diagnosis)</term><term>Hemangiosarcoma (pathology)</term><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></keywords><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><term>Tumeurs cutanées ()</term><term>Tumeurs cutanées (anatomopathologie)</term><term>Tumeurs cutanées (diagnostic)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Hémangiosarcome</term><term>Tumeurs cutanées</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Hémangiosarcome</term><term>Tumeurs cutanées</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term><term>Female</term><term>Humans</term><term>Middle Aged</term><term>Thigh</term></keywords><keywords scheme="MESH" 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>Tumeurs cutanées</term></keywords></textClass></profileDesc></teiHeader><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></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20409411</PMID><DateCreated><Year>2010</Year><Month>04</Month><Day>22</Day></DateCreated><DateCompleted><Year>2010</Year><Month>07</Month><Day>22</Day></DateCompleted><DateRevised><Year>2010</Year><Month>04</Month><Day>22</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1087-2108</ISSN><JournalIssue CitedMedium="Internet"><Volume>16</Volume><Issue>4</Issue><PubDate><Year>2010</Year><Month>Apr</Month><Day>15</Day></PubDate></JournalIssue><Title>Dermatology online journal</Title><ISOAbbreviation>Dermatol. Online J.</ISOAbbreviation></Journal><ArticleTitle>Papillary intralymphatic angioendothelioma of the thigh: A case report and review of the literature.</ArticleTitle><Pagination><MedlinePgn>4</MedlinePgn></Pagination><Abstract><AbstractText>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.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ward</LastName><ForeName>Katherine A</ForeName><Initials>KA</Initials><AffiliationInfo><Affiliation>University of Minnesota, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ecker</LastName><ForeName>Phillip M</ForeName><Initials>PM</Initials></Author><Author ValidYN="Y"><LastName>White</LastName><ForeName>Rebekah R</ForeName><Initials>RR</Initials></Author><Author ValidYN="Y"><LastName>Melnik</LastName><ForeName>Tanya E</ForeName><Initials>TE</Initials></Author><Author ValidYN="Y"><LastName>Gulbahce</LastName><ForeName>Evin H</ForeName><Initials>EH</Initials></Author><Author ValidYN="Y"><LastName>Wilke</LastName><ForeName>Mark S</ForeName><Initials>MS</Initials></Author><Author ValidYN="Y"><LastName>Sangueza</LastName><ForeName>Omar P</ForeName><Initials>OP</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2010</Year><Month>04</Month><Day>15</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Dermatol Online J</MedlineTA><NlmUniqueID>9610776</NlmUniqueID><ISSNLinking>1087-2108</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D003937" MajorTopicYN="N">Diagnosis, Differential</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013848" MajorTopicYN="Y">Thigh</DescriptorName></MeshHeading></MeshHeadingList><NumberOfReferences>27</NumberOfReferences></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2010</Year><Month>4</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2010</Year><Month>4</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2010</Year><Month>7</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">20409411</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country></list><tree><noCountry><name sortKey="Ecker, Phillip M" sort="Ecker, Phillip M" uniqKey="Ecker P" first="Phillip M" last="Ecker">Phillip M. Ecker</name><name sortKey="Gulbahce, Evin H" sort="Gulbahce, Evin H" uniqKey="Gulbahce E" first="Evin H" last="Gulbahce">Evin H. Gulbahce</name><name sortKey="Melnik, Tanya E" sort="Melnik, Tanya E" uniqKey="Melnik T" first="Tanya E" last="Melnik">Tanya E. Melnik</name><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></noCountry><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></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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