Case of angiosarcoma on the abdominal wall, an extremely rare variant, putatively shared the pathogenesis with Stewart-Treves syndrome.
Identifieur interne : 007059 ( Ncbi/Merge ); précédent : 007058; suivant : 007060Case of angiosarcoma on the abdominal wall, an extremely rare variant, putatively shared the pathogenesis with Stewart-Treves syndrome.
Auteurs : Misaki Ise [Japon] ; Takeru Funakoshi ; Yuki Furuichi ; Haruki Honda ; Yumi Fujio ; Masayuki Amagai ; Manabu OhyamaSource :
- The Journal of dermatology [ 1346-8138 ] ; 2015.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Hémangiosarcome, Lymphangiosarcome, Tumeurs cutanées.
- étiologie : Hémangiosarcome, Lymphangiosarcome, Tumeurs cutanées.
- Femelle, Humains, Lymphoedème, Paroi abdominale, Sujet âgé.
English descriptors
- KwdEn :
- MESH :
- complications : Lymphedema.
- etiology : Hemangiosarcoma, Lymphangiosarcoma, Skin Neoplasms.
- pathology : Hemangiosarcoma, Lymphangiosarcoma, Skin Neoplasms.
- Abdominal Wall, Aged, Female, Humans.
DOI: 10.1111/1346-8138.12809
PubMed: 25703383
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pubmed:25703383Le document en format XML
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Dermatol.</ISOAbbreviation></Journal><ArticleTitle>Case of angiosarcoma on the abdominal wall, an extremely rare variant, putatively shared the pathogenesis with Stewart-Treves syndrome.</ArticleTitle><Pagination><MedlinePgn>426-7</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/1346-8138.12809</ELocationID><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ise</LastName><ForeName>Misaki</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Funakoshi</LastName><ForeName>Takeru</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Furuichi</LastName><ForeName>Yuki</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Honda</LastName><ForeName>Haruki</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Fujio</LastName><ForeName>Yumi</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Amagai</LastName><ForeName>Masayuki</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Ohyama</LastName><ForeName>Manabu</ForeName><Initials>M</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016422">Letter</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>02</Month><Day>21</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>J Dermatol</MedlineTA><NlmUniqueID>7600545</NlmUniqueID><ISSNLinking>0385-2407</ISSNLinking></MedlineJournalInfo><SupplMeshList><SupplMeshName Type="Disease" UI="C537491">Stewart Treves syndrome</SupplMeshName></SupplMeshList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D034861" MajorTopicYN="N">Abdominal Wall</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2015</Year><Month>2</Month><Day>24</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2015</Year><Month>2</Month><Day>24</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2016</Year><Month>12</Month><Day>15</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">25703383</ArticleId><ArticleId IdType="doi">10.1111/1346-8138.12809</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Japon</li></country><region><li>Région de Kantō</li></region><settlement><li>Tokyo</li></settlement></list><tree><noCountry><name sortKey="Amagai, Masayuki" sort="Amagai, Masayuki" uniqKey="Amagai M" first="Masayuki" last="Amagai">Masayuki Amagai</name><name sortKey="Fujio, Yumi" sort="Fujio, Yumi" uniqKey="Fujio Y" first="Yumi" last="Fujio">Yumi Fujio</name><name sortKey="Funakoshi, Takeru" sort="Funakoshi, Takeru" uniqKey="Funakoshi T" first="Takeru" last="Funakoshi">Takeru Funakoshi</name><name sortKey="Furuichi, Yuki" sort="Furuichi, Yuki" uniqKey="Furuichi Y" first="Yuki" last="Furuichi">Yuki Furuichi</name><name sortKey="Honda, Haruki" sort="Honda, Haruki" uniqKey="Honda H" first="Haruki" last="Honda">Haruki Honda</name><name sortKey="Ohyama, Manabu" sort="Ohyama, Manabu" uniqKey="Ohyama M" first="Manabu" last="Ohyama">Manabu Ohyama</name></noCountry><country name="Japon"><region name="Région de Kantō"><name sortKey="Ise, Misaki" sort="Ise, Misaki" uniqKey="Ise M" first="Misaki" last="Ise">Misaki Ise</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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