Angiosarcoma arising in a lymphedematous abdominal pannus with histologic features reminiscent of Kaposi's sarcoma: report of a case and review of the literature.
Identifieur interne : 003A00 ( PubMed/Curation ); précédent : 003999; suivant : 003A01Angiosarcoma arising in a lymphedematous abdominal pannus with histologic features reminiscent of Kaposi's sarcoma: report of a case and review of the literature.
Auteurs : James M. Shehan [États-Unis] ; Iftikhar AhmedSource :
- International journal of dermatology [ 0011-9059 ] ; 2006.
Descripteurs français
- KwdFr :
- Abdomen (anatomopathologie), Diagnostic différentiel, Femelle, Humains, Hémangiosarcome (diagnostic), Hémangiosarcome (secondaire), Hémangiosarcome (traitement médicamenteux), Issue fatale, Obésité morbide, Oedème, Protocoles de polychimiothérapie antinéoplasique (usage thérapeutique), Sarcome de Kaposi (diagnostic), Sujet âgé, Sujet âgé de 80 ans ou plus, Tumeurs cutanées (anatomopathologie), Tumeurs cutanées (diagnostic), Tumeurs cutanées (traitement médicamenteux), Tumeurs du poumon (diagnostic), Tumeurs du poumon (secondaire), Tumeurs du poumon (traitement médicamenteux).
- MESH :
- anatomopathologie : Abdomen, Tumeurs cutanées.
- diagnostic : Hémangiosarcome, Sarcome de Kaposi, Tumeurs cutanées, Tumeurs du poumon.
- secondaire : Hémangiosarcome, Tumeurs du poumon.
- traitement médicamenteux : Hémangiosarcome, Tumeurs cutanées, Tumeurs du poumon.
- usage thérapeutique : Protocoles de polychimiothérapie antinéoplasique.
- Diagnostic différentiel, Femelle, Humains, Issue fatale, Obésité morbide, Oedème, Sujet âgé, Sujet âgé de 80 ans ou plus.
English descriptors
- KwdEn :
- Abdomen (pathology), Aged, Aged, 80 and over, Antineoplastic Combined Chemotherapy Protocols (therapeutic use), Diagnosis, Differential, Edema, Fatal Outcome, Female, Hemangiosarcoma (diagnosis), Hemangiosarcoma (drug therapy), Hemangiosarcoma (secondary), Humans, Lung Neoplasms (diagnosis), Lung Neoplasms (drug therapy), Lung Neoplasms (secondary), Obesity, Morbid, Sarcoma, Kaposi (diagnosis), Skin Neoplasms (diagnosis), Skin Neoplasms (drug therapy), Skin Neoplasms (pathology).
- MESH :
- diagnosis : Hemangiosarcoma, Lung Neoplasms, Sarcoma, Kaposi, Skin Neoplasms.
- drug therapy : Hemangiosarcoma, Lung Neoplasms, Skin Neoplasms.
- pathology : Abdomen, Skin Neoplasms.
- secondary : Hemangiosarcoma, Lung Neoplasms.
- therapeutic use : Antineoplastic Combined Chemotherapy Protocols.
- Aged, Aged, 80 and over, Diagnosis, Differential, Edema, Fatal Outcome, Female, Humans, Obesity, Morbid.
Abstract
Despite common endothelial origins, angiosarcoma and Kaposi's sarcoma are clinically and histologically distinct vascular proliferations. The development of angiosarcoma in a chronically edematous abdominal pannus is extremely uncommon. Similarly, tumors with the combined histologic features of angiosarcoma and Kaposi's sarcoma have rarely been described.
DOI: 10.1111/j.1365-4632.2004.02560.x
PubMed: 16700780
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Shehan</name><affiliation wicri:level="1"><nlm:affiliation>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905</wicri:regionArea></affiliation></author><author><name sortKey="Ahmed, Iftikhar" sort="Ahmed, Iftikhar" uniqKey="Ahmed I" first="Iftikhar" last="Ahmed">Iftikhar Ahmed</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2006">2006</date><idno type="RBID">pubmed:16700780</idno><idno type="pmid">16700780</idno><idno type="doi">10.1111/j.1365-4632.2004.02560.x</idno><idno type="wicri:Area/PubMed/Corpus">003A00</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">003A00</idno><idno type="wicri:Area/PubMed/Curation">003A00</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">003A00</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Angiosarcoma arising in a lymphedematous abdominal pannus with histologic features reminiscent of Kaposi's sarcoma: report of a case and review of the literature.</title><author><name sortKey="Shehan, James M" sort="Shehan, James M" uniqKey="Shehan J" first="James M" last="Shehan">James M. Shehan</name><affiliation wicri:level="1"><nlm:affiliation>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905</wicri:regionArea></affiliation></author><author><name sortKey="Ahmed, Iftikhar" sort="Ahmed, Iftikhar" uniqKey="Ahmed I" first="Iftikhar" last="Ahmed">Iftikhar Ahmed</name></author></analytic><series><title level="j">International journal of dermatology</title><idno type="ISSN">0011-9059</idno><imprint><date when="2006" type="published">2006</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abdomen (pathology)</term><term>Aged</term><term>Aged, 80 and over</term><term>Antineoplastic Combined Chemotherapy Protocols (therapeutic use)</term><term>Diagnosis, Differential</term><term>Edema</term><term>Fatal Outcome</term><term>Female</term><term>Hemangiosarcoma (diagnosis)</term><term>Hemangiosarcoma (drug therapy)</term><term>Hemangiosarcoma (secondary)</term><term>Humans</term><term>Lung Neoplasms (diagnosis)</term><term>Lung Neoplasms (drug therapy)</term><term>Lung Neoplasms (secondary)</term><term>Obesity, Morbid</term><term>Sarcoma, Kaposi (diagnosis)</term><term>Skin Neoplasms (diagnosis)</term><term>Skin Neoplasms (drug therapy)</term><term>Skin Neoplasms (pathology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Abdomen (anatomopathologie)</term><term>Diagnostic différentiel</term><term>Femelle</term><term>Humains</term><term>Hémangiosarcome (diagnostic)</term><term>Hémangiosarcome (secondaire)</term><term>Hémangiosarcome (traitement médicamenteux)</term><term>Issue fatale</term><term>Obésité morbide</term><term>Oedème</term><term>Protocoles de polychimiothérapie antinéoplasique (usage thérapeutique)</term><term>Sarcome de Kaposi (diagnostic)</term><term>Sujet âgé</term><term>Sujet âgé de 80 ans ou plus</term><term>Tumeurs cutanées (anatomopathologie)</term><term>Tumeurs cutanées (diagnostic)</term><term>Tumeurs cutanées (traitement médicamenteux)</term><term>Tumeurs du poumon (diagnostic)</term><term>Tumeurs du poumon (secondaire)</term><term>Tumeurs du poumon (traitement médicamenteux)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Abdomen</term><term>Tumeurs cutanées</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Hemangiosarcoma</term><term>Lung Neoplasms</term><term>Sarcoma, Kaposi</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Hémangiosarcome</term><term>Sarcome de Kaposi</term><term>Tumeurs cutanées</term><term>Tumeurs du poumon</term></keywords><keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Hemangiosarcoma</term><term>Lung Neoplasms</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Abdomen</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="secondaire" xml:lang="fr"><term>Hémangiosarcome</term><term>Tumeurs du poumon</term></keywords><keywords scheme="MESH" qualifier="secondary" xml:lang="en"><term>Hemangiosarcoma</term><term>Lung Neoplasms</term></keywords><keywords scheme="MESH" qualifier="therapeutic use" xml:lang="en"><term>Antineoplastic Combined Chemotherapy Protocols</term></keywords><keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr"><term>Hémangiosarcome</term><term>Tumeurs cutanées</term><term>Tumeurs du poumon</term></keywords><keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Protocoles de polychimiothérapie antinéoplasique</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Aged, 80 and over</term><term>Diagnosis, Differential</term><term>Edema</term><term>Fatal Outcome</term><term>Female</term><term>Humans</term><term>Obesity, Morbid</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Diagnostic différentiel</term><term>Femelle</term><term>Humains</term><term>Issue fatale</term><term>Obésité morbide</term><term>Oedème</term><term>Sujet âgé</term><term>Sujet âgé de 80 ans ou plus</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Despite common endothelial origins, angiosarcoma and Kaposi's sarcoma are clinically and histologically distinct vascular proliferations. The development of angiosarcoma in a chronically edematous abdominal pannus is extremely uncommon. Similarly, tumors with the combined histologic features of angiosarcoma and Kaposi's sarcoma have rarely been described.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16700780</PMID><DateCreated><Year>2006</Year><Month>05</Month><Day>16</Day></DateCreated><DateCompleted><Year>2006</Year><Month>10</Month><Day>24</Day></DateCompleted><DateRevised><Year>2007</Year><Month>08</Month><Day>03</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0011-9059</ISSN><JournalIssue CitedMedium="Print"><Volume>45</Volume><Issue>5</Issue><PubDate><Year>2006</Year><Month>May</Month></PubDate></JournalIssue><Title>International journal of dermatology</Title><ISOAbbreviation>Int. J. Dermatol.</ISOAbbreviation></Journal><ArticleTitle>Angiosarcoma arising in a lymphedematous abdominal pannus with histologic features reminiscent of Kaposi's sarcoma: report of a case and review of the literature.</ArticleTitle><Pagination><MedlinePgn>499-503</MedlinePgn></Pagination><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Despite common endothelial origins, angiosarcoma and Kaposi's sarcoma are clinically and histologically distinct vascular proliferations. The development of angiosarcoma in a chronically edematous abdominal pannus is extremely uncommon. Similarly, tumors with the combined histologic features of angiosarcoma and Kaposi's sarcoma have rarely been described.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">We reviewed the literature on angiosarcoma arising in a lymphedematous abdominal pannus and evaluated an 81-year-old morbidly obese woman who had profound, long-standing edema of the lower abdominal wall in which an aggressive vascular tumor developed.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Three clinically similar cases were identified in the literature. All patients were women who generally experienced rapid disease progression. In addition, in our patient, sequential cutaneous sampling from different lesional sites demonstrated disparate histologic changes, ranging from those of classic Kaposi's sarcoma to high-grade angiosarcoma, to areas with combined features of the two tumors. A polymerase chain reaction performed on lesional tissue was negative for human herpesvirus-8 DNA.</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">It is important to note that angiosarcoma may develop in the abdomen in association with chronic lymphedema, as demonstrated by the cases noted in this report. In addition, our case highlights the difficulty in differentiating histologically angiosarcoma from Kaposi's sarcoma in some situations, and demonstrates the value of close clinicopathologic correlation and sequential tissue sampling in evaluating problematic cases.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Shehan</LastName><ForeName>James M</ForeName><Initials>JM</Initials><AffiliationInfo><Affiliation>Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ahmed</LastName><ForeName>Iftikhar</ForeName><Initials>I</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>England</Country><MedlineTA>Int J Dermatol</MedlineTA><NlmUniqueID>0243704</NlmUniqueID><ISSNLinking>0011-9059</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="CommentIn"><RefSource>Int J Dermatol. 2007 Jun;46(6):662</RefSource><PMID Version="1">17550576</PMID></CommentsCorrections></CommentsCorrectionsList><MeshHeadingList><MeshHeading><DescriptorName UI="D000005" MajorTopicYN="N">Abdomen</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000369" MajorTopicYN="N">Aged, 80 and over</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000971" MajorTopicYN="N">Antineoplastic Combined Chemotherapy Protocols</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003937" MajorTopicYN="N">Diagnosis, Differential</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004487" MajorTopicYN="Y">Edema</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017809" MajorTopicYN="N">Fatal Outcome</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="Q000188" MajorTopicYN="N">drug therapy</QualifierName><QualifierName UI="Q000556" MajorTopicYN="N">secondary</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008175" MajorTopicYN="N">Lung Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000188" MajorTopicYN="N">drug therapy</QualifierName><QualifierName UI="Q000556" MajorTopicYN="N">secondary</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009767" MajorTopicYN="Y">Obesity, Morbid</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012514" MajorTopicYN="N">Sarcoma, Kaposi</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000188" MajorTopicYN="N">drug therapy</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading></MeshHeadingList><NumberOfReferences>21</NumberOfReferences></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year><Month>5</Month><Day>17</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2006</Year><Month>10</Month><Day>25</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2006</Year><Month>5</Month><Day>17</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16700780</ArticleId><ArticleId IdType="pii">IJD2560</ArticleId><ArticleId IdType="doi">10.1111/j.1365-4632.2004.02560.x</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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