Cutaneous angiosarcoma of the foot: a case report and review of the literature.
Identifieur interne : 001098 ( PubMed/Corpus ); précédent : 001097; suivant : 001099Cutaneous angiosarcoma of the foot: a case report and review of the literature.
Auteurs : Sharang Tenjarla ; Lucy Ashley Sheils ; Theresa M. Kwiatkowski ; Sheema ChawlaSource :
- Case reports in oncological medicine [ 2090-6706 ] ; 2014.
Abstract
Primary Angiosarcoma of the skin of the foot is very rare. Angiosarcoma is typically treated with resection and wide-field postoperative radiation therapy. Chemotherapy and radiation therapy have also been used. Regardless of the treatment, the risk of local and distant relapse remains high for this disease. We present a case of an elderly patient who developed cutaneous angiosarcoma of the foot. It posed as a diagnostic dilemma at presentation. Chronic lymphedema was a possible predisposing factor. Given his age, preexisting renal dysfunction, refusal of surgery, and preference not to receive chemotherapy, the patient was ultimately treated with definitive radiotherapy. We present this case because of its rare site, unique presentation and delay in diagnosis of the condition, and attainment of an excellent response to radiation at the time of follow-up. We also review the current literature on this topic.
DOI: 10.1155/2014/657876
PubMed: 25574410
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Kwiatkowski</name><affiliation><nlm:affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Chawla, Sheema" sort="Chawla, Sheema" uniqKey="Chawla S" first="Sheema" last="Chawla">Sheema Chawla</name><affiliation><nlm:affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2014">2014</date><idno type="RBID">pubmed:25574410</idno><idno type="pmid">25574410</idno><idno type="doi">10.1155/2014/657876</idno><idno type="wicri:Area/PubMed/Corpus">001098</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001098</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Cutaneous angiosarcoma of the foot: a case report and review of the literature.</title><author><name sortKey="Tenjarla, Sharang" sort="Tenjarla, Sharang" uniqKey="Tenjarla S" first="Sharang" last="Tenjarla">Sharang Tenjarla</name><affiliation><nlm:affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Sheils, Lucy Ashley" sort="Sheils, Lucy Ashley" uniqKey="Sheils L" first="Lucy Ashley" last="Sheils">Lucy Ashley Sheils</name><affiliation><nlm:affiliation>Department of Pathology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Kwiatkowski, Theresa M" sort="Kwiatkowski, Theresa M" uniqKey="Kwiatkowski T" first="Theresa M" last="Kwiatkowski">Theresa M. Kwiatkowski</name><affiliation><nlm:affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Chawla, Sheema" sort="Chawla, Sheema" uniqKey="Chawla S" first="Sheema" last="Chawla">Sheema Chawla</name><affiliation><nlm:affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Case reports in oncological medicine</title><idno type="ISSN">2090-6706</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Primary Angiosarcoma of the skin of the foot is very rare. Angiosarcoma is typically treated with resection and wide-field postoperative radiation therapy. Chemotherapy and radiation therapy have also been used. Regardless of the treatment, the risk of local and distant relapse remains high for this disease. We present a case of an elderly patient who developed cutaneous angiosarcoma of the foot. It posed as a diagnostic dilemma at presentation. Chronic lymphedema was a possible predisposing factor. Given his age, preexisting renal dysfunction, refusal of surgery, and preference not to receive chemotherapy, the patient was ultimately treated with definitive radiotherapy. We present this case because of its rare site, unique presentation and delay in diagnosis of the condition, and attainment of an excellent response to radiation at the time of follow-up. We also review the current literature on this topic.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">25574410</PMID><DateCreated><Year>2015</Year><Month>01</Month><Day>09</Day></DateCreated><DateCompleted><Year>2015</Year><Month>01</Month><Day>09</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>20</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">2090-6706</ISSN><JournalIssue CitedMedium="Print"><Volume>2014</Volume><PubDate><Year>2014</Year></PubDate></JournalIssue><Title>Case reports in oncological medicine</Title><ISOAbbreviation>Case Rep Oncol Med</ISOAbbreviation></Journal><ArticleTitle>Cutaneous angiosarcoma of the foot: a case report and review of the literature.</ArticleTitle><Pagination><MedlinePgn>657876</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1155/2014/657876</ELocationID><Abstract><AbstractText>Primary Angiosarcoma of the skin of the foot is very rare. Angiosarcoma is typically treated with resection and wide-field postoperative radiation therapy. Chemotherapy and radiation therapy have also been used. Regardless of the treatment, the risk of local and distant relapse remains high for this disease. We present a case of an elderly patient who developed cutaneous angiosarcoma of the foot. It posed as a diagnostic dilemma at presentation. Chronic lymphedema was a possible predisposing factor. Given his age, preexisting renal dysfunction, refusal of surgery, and preference not to receive chemotherapy, the patient was ultimately treated with definitive radiotherapy. We present this case because of its rare site, unique presentation and delay in diagnosis of the condition, and attainment of an excellent response to radiation at the time of follow-up. We also review the current literature on this topic.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tenjarla</LastName><ForeName>Sharang</ForeName><Initials>S</Initials><Identifier Source="ORCID">0000-0002-5180-0003</Identifier><AffiliationInfo><Affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sheils</LastName><ForeName>Lucy Ashley</ForeName><Initials>LA</Initials><AffiliationInfo><Affiliation>Department of Pathology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kwiatkowski</LastName><ForeName>Theresa M</ForeName><Initials>TM</Initials><AffiliationInfo><Affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chawla</LastName><ForeName>Sheema</ForeName><Initials>S</Initials><Identifier Source="ORCID">0000-0002-9279-8552</Identifier><AffiliationInfo><Affiliation>Department of Radiation Oncology, Rochester General Hospital, 1425 Portland Avenue, Rochester, NY 14621, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>12</Month><Day>09</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Case Rep Oncol Med</MedlineTA><NlmUniqueID>101581035</NlmUniqueID></MedlineJournalInfo><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>J Surg Oncol. 1996 Mar;61(3):170-6</RefSource><PMID Version="1">8637202</PMID></CommentsCorrections><CommentsCorrections 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