Angiosarcoma: a case report and review of the literature.
Identifieur interne : 003B05 ( PubMed/Curation ); précédent : 003B04; suivant : 003B06Angiosarcoma: a case report and review of the literature.
Auteurs : Abdulhafez Selim [États-Unis] ; Amor Khachemoune ; Norman A. LockshinSource :
- Cutis [ 0011-4162 ] ; 2005.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Nez.
- diagnostic : Hémangiosarcome, Tumeurs cutanées.
- Diagnostic différentiel, Humains, Hémangiosarcome, Mâle, Nez, Radiothérapie adjuvante, Sujet âgé de 80 ans ou plus, Tumeurs cutanées.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Hemangiosarcoma, Skin Neoplasms.
- pathology : Nose.
- surgery : Nose.
- therapy : Hemangiosarcoma, Skin Neoplasms.
- Aged, 80 and over, Diagnosis, Differential, Humans, Male, Radiotherapy, Adjuvant.
Abstract
Angiosarcoma is an aggressive neoplasm that predominantly affects elderly patients. Most cases appear on the scalp and face de novo; however, trauma, longstanding lymphedema, and irradiation are predisposing factors. Management includes a multidisciplinary team and may involve a combination of surgery, radiation, and chemotherapy tailored to the patient's age and associated comorbidities.
PubMed: 16422466
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Lockshin</name></author></analytic><series><title level="j">Cutis</title><idno type="ISSN">0011-4162</idno><imprint><date when="2005" type="published">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged, 80 and over</term><term>Diagnosis, Differential</term><term>Hemangiosarcoma (diagnosis)</term><term>Hemangiosarcoma (therapy)</term><term>Humans</term><term>Male</term><term>Nose (pathology)</term><term>Nose (surgery)</term><term>Radiotherapy, Adjuvant</term><term>Skin Neoplasms (diagnosis)</term><term>Skin Neoplasms (therapy)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Diagnostic différentiel</term><term>Humains</term><term>Hémangiosarcome ()</term><term>Hémangiosarcome (diagnostic)</term><term>Mâle</term><term>Nez ()</term><term>Nez (anatomopathologie)</term><term>Radiothérapie adjuvante</term><term>Sujet âgé de 80 ans ou plus</term><term>Tumeurs cutanées ()</term><term>Tumeurs cutanées (diagnostic)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Nez</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>Nose</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Nose</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged, 80 and over</term><term>Diagnosis, Differential</term><term>Humans</term><term>Male</term><term>Radiotherapy, Adjuvant</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Diagnostic différentiel</term><term>Humains</term><term>Hémangiosarcome</term><term>Mâle</term><term>Nez</term><term>Radiothérapie adjuvante</term><term>Sujet âgé de 80 ans ou plus</term><term>Tumeurs cutanées</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Angiosarcoma is an aggressive neoplasm that predominantly affects elderly patients. Most cases appear on the scalp and face de novo; however, trauma, longstanding lymphedema, and irradiation are predisposing factors. Management includes a multidisciplinary team and may involve a combination of surgery, radiation, and chemotherapy tailored to the patient's age and associated comorbidities.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16422466</PMID><DateCreated><Year>2006</Year><Month>01</Month><Day>20</Day></DateCreated><DateCompleted><Year>2006</Year><Month>03</Month><Day>23</Day></DateCompleted><DateRevised><Year>2013</Year><Month>09</Month><Day>12</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0011-4162</ISSN><JournalIssue CitedMedium="Print"><Volume>76</Volume><Issue>5</Issue><PubDate><Year>2005</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Cutis</Title><ISOAbbreviation>Cutis</ISOAbbreviation></Journal><ArticleTitle>Angiosarcoma: a case report and review of the literature.</ArticleTitle><Pagination><MedlinePgn>313-7</MedlinePgn></Pagination><Abstract><AbstractText>Angiosarcoma is an aggressive neoplasm that predominantly affects elderly patients. Most cases appear on the scalp and face de novo; however, trauma, longstanding lymphedema, and irradiation are predisposing factors. Management includes a multidisciplinary team and may involve a combination of surgery, radiation, and chemotherapy tailored to the patient's age and associated comorbidities.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Selim</LastName><ForeName>Abdulhafez</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Endocrine Unit, Department of Internal Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, USA. amorkh@pol.net</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Khachemoune</LastName><ForeName>Amor</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Lockshin</LastName><ForeName>Norman A</ForeName><Initials>NA</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></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Cutis</MedlineTA><NlmUniqueID>0006440</NlmUniqueID><ISSNLinking>0011-4162</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000369" MajorTopicYN="N">Aged, 80 and over</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003937" MajorTopicYN="N">Diagnosis, Differential</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009666" MajorTopicYN="N">Nose</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018714" MajorTopicYN="N">Radiotherapy, Adjuvant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading></MeshHeadingList><NumberOfReferences>28</NumberOfReferences></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year><Month>1</Month><Day>21</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2006</Year><Month>3</Month><Day>24</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2006</Year><Month>1</Month><Day>21</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16422466</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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