Angiosarcoma of penis: Case report of an aggressive penile cancer
Identifieur interne : 002407 ( Pmc/Curation ); précédent : 002406; suivant : 002408Angiosarcoma of penis: Case report of an aggressive penile cancer
Auteurs : Vinod Priyadarshi [Inde] ; Hemant Kumar Goel [Inde] ; Debashish Chakrabarty [Inde] ; Dilip Kumar Pal [Inde]Source :
- Urology Annals [ 0974-7796 ] ; 2015.
Abstract
Angiosarcoma is a very rare mesenchymal tumor of penis. Though extremely unusual, it should be considered in the differential diagnosis in patients presenting with a penile growth or a localized subcutaneous penile lesions as they are very aggressive and there is a high chance of recurrence. One such case is reported here, which was aggressively treated with total penectomy and the patient did not show any recurrence in 2 years of follow-up.
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DOI: 10.4103/0974-7796.150497
PubMed: 25837261
PubMed Central: 4374270
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<front><div type="abstract" xml:lang="en"><p>Angiosarcoma is a very rare mesenchymal tumor of penis. Though extremely unusual, it should be considered in the differential diagnosis in patients presenting with a penile growth or a localized subcutaneous penile lesions as they are very aggressive and there is a high chance of recurrence. One such case is reported here, which was aggressively treated with total penectomy and the patient did not show any recurrence in 2 years of follow-up.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Urol Ann</journal-id>
<journal-id journal-id-type="iso-abbrev">Urol Ann</journal-id>
<journal-id journal-id-type="publisher-id">UA</journal-id>
<journal-title-group><journal-title>Urology Annals</journal-title>
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<article-id pub-id-type="doi">10.4103/0974-7796.150497</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
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<title-group><article-title>Angiosarcoma of penis: Case report of an aggressive penile cancer</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Priyadarshi</surname>
<given-names>Vinod</given-names>
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<xref ref-type="aff" rid="aff1"></xref>
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<contrib contrib-type="author"><name><surname>Goel</surname>
<given-names>Hemant Kumar</given-names>
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<contrib contrib-type="author"><name><surname>Chakrabarty</surname>
<given-names>Debashish</given-names>
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<xref ref-type="aff" rid="aff2">1</xref>
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<contrib contrib-type="author"><name><surname>Pal</surname>
<given-names>Dilip Kumar</given-names>
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<aff id="aff1">Department of Urology, IPGMER and SSKM Hospital, Kolkata, West Bengal, India</aff>
<aff id="aff2"><label>1</label>
Department of Pathology, IPGMER and SSKM Hospital, Kolkata, West Bengal, India</aff>
<author-notes><corresp id="cor1"><bold>Address for correspondence:</bold>
Dr. Vinod Priyadarshi, Department of Urology, IPGMER and SSKM Hospital, Kolkata - 700 020, India. E-mail: <email xlink:href="vinod_priyadarshi@yahoo.com">vinod_priyadarshi@yahoo.com</email>
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<pub-date pub-type="ppub"><season>Apr-Jun</season>
<year>2015</year>
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<volume>7</volume>
<issue>2</issue>
<fpage>251</fpage>
<lpage>253</lpage>
<history><date date-type="received"><day>27</day>
<month>5</month>
<year>2013</year>
</date>
<date date-type="accepted"><day>25</day>
<month>9</month>
<year>2013</year>
</date>
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<permissions><copyright-statement>Copyright: © Urology Annals</copyright-statement>
<copyright-year>2015</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/3.0"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract><p>Angiosarcoma is a very rare mesenchymal tumor of penis. Though extremely unusual, it should be considered in the differential diagnosis in patients presenting with a penile growth or a localized subcutaneous penile lesions as they are very aggressive and there is a high chance of recurrence. One such case is reported here, which was aggressively treated with total penectomy and the patient did not show any recurrence in 2 years of follow-up.</p>
</abstract>
<kwd-group><kwd>Angiosarcoma</kwd>
<kwd>mesenchymal tumor</kwd>
<kwd>penis</kwd>
</kwd-group>
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