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<title xml:lang="en">Primary Angiosarcoma of Breast: A Case Report</title>
<author>
<name sortKey="Raju, K V V N" sort="Raju, K V V N" uniqKey="Raju K" first="K. V. V. N." last="Raju">K. V. V. N. Raju</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Mahajan, Munish" sort="Mahajan, Munish" uniqKey="Mahajan M" first="Munish" last="Mahajan">Munish Mahajan</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
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<author>
<name sortKey="Rehmani, Kabir" sort="Rehmani, Kabir" uniqKey="Rehmani K" first="Kabir" last="Rehmani">Kabir Rehmani</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
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<author>
<name sortKey="Pawar, Satish" sort="Pawar, Satish" uniqKey="Pawar S" first="Satish" last="Pawar">Satish Pawar</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Murthy, Sudha S" sort="Murthy, Sudha S" uniqKey="Murthy S" first="Sudha S." last="Murthy">Sudha S. Murthy</name>
<affiliation>
<nlm:aff id="Aff2">Department of Laboratory Medicine, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
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<idno type="doi">10.1007/s13193-014-0302-y</idno>
<date when="2014">2014</date>
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<title xml:lang="en" level="a" type="main">Primary Angiosarcoma of Breast: A Case Report</title>
<author>
<name sortKey="Raju, K V V N" sort="Raju, K V V N" uniqKey="Raju K" first="K. V. V. N." last="Raju">K. V. V. N. Raju</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Mahajan, Munish" sort="Mahajan, Munish" uniqKey="Mahajan M" first="Munish" last="Mahajan">Munish Mahajan</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Rehmani, Kabir" sort="Rehmani, Kabir" uniqKey="Rehmani K" first="Kabir" last="Rehmani">Kabir Rehmani</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Pawar, Satish" sort="Pawar, Satish" uniqKey="Pawar S" first="Satish" last="Pawar">Satish Pawar</name>
<affiliation>
<nlm:aff id="Aff1">Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Murthy, Sudha S" sort="Murthy, Sudha S" uniqKey="Murthy S" first="Sudha S." last="Murthy">Sudha S. Murthy</name>
<affiliation>
<nlm:aff id="Aff2">Department of Laboratory Medicine, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</nlm:aff>
</affiliation>
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<series>
<title level="j">Indian Journal of Surgical Oncology</title>
<idno type="ISSN">0975-7651</idno>
<idno type="eISSN">0976-6952</idno>
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<date when="2014">2014</date>
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<div type="abstract" xml:lang="en">
<p>Primary breast sarcomas are rare entities. These malignant tumors originate from mesenchymal glandular breast tissue and account for
<italic><</italic>
1 % of all breast cancer cases. Angiosarcomas are rare malignant tumors that arise from endothelial cells lining vascular channels. Most angiosarcomas are secondary to radiotherapy treatments for breast cancer or to an arm lymphoedema subsequent to a modified radical mastectomy. Primary angiosarcomas are rare and account for 0.04 % of all malignant breast tumors.</p>
</div>
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<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
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<journal-meta>
<journal-id journal-id-type="nlm-ta">Indian J Surg Oncol</journal-id>
<journal-id journal-id-type="iso-abbrev">Indian J Surg Oncol</journal-id>
<journal-title-group>
<journal-title>Indian Journal of Surgical Oncology</journal-title>
</journal-title-group>
<issn pub-type="ppub">0975-7651</issn>
<issn pub-type="epub">0976-6952</issn>
<publisher>
<publisher-name>Springer India</publisher-name>
<publisher-loc>India</publisher-loc>
</publisher>
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<article-id pub-id-type="pmid">25114472</article-id>
<article-id pub-id-type="pmc">4116542</article-id>
<article-id pub-id-type="publisher-id">302</article-id>
<article-id pub-id-type="doi">10.1007/s13193-014-0302-y</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Primary Angiosarcoma of Breast: A Case Report</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Raju</surname>
<given-names>K. V. V. N.</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Mahajan</surname>
<given-names>Munish</given-names>
</name>
<address>
<phone>+91-9963592932</phone>
<fax>+91-40-23542120</fax>
<email>mahajan0134@gmail.com</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rehmani</surname>
<given-names>Kabir</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pawar</surname>
<given-names>Satish</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Murthy</surname>
<given-names>Sudha S.</given-names>
</name>
<xref ref-type="aff" rid="Aff2"></xref>
</contrib>
<aff id="Aff1">
<label></label>
Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</aff>
<aff id="Aff2">
<label></label>
Department of Laboratory Medicine, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 500034</aff>
</contrib-group>
<pub-date pub-type="epub">
<day>9</day>
<month>4</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="ppub">
<month>6</month>
<year>2014</year>
</pub-date>
<volume>5</volume>
<issue>2</issue>
<fpage>155</fpage>
<lpage>157</lpage>
<history>
<date date-type="received">
<day>19</day>
<month>9</month>
<year>2013</year>
</date>
<date date-type="accepted">
<day>10</day>
<month>3</month>
<year>2014</year>
</date>
</history>
<permissions>
<copyright-statement>© Indian Association of Surgical Oncology 2014</copyright-statement>
</permissions>
<abstract id="Abs1">
<p>Primary breast sarcomas are rare entities. These malignant tumors originate from mesenchymal glandular breast tissue and account for
<italic><</italic>
1 % of all breast cancer cases. Angiosarcomas are rare malignant tumors that arise from endothelial cells lining vascular channels. Most angiosarcomas are secondary to radiotherapy treatments for breast cancer or to an arm lymphoedema subsequent to a modified radical mastectomy. Primary angiosarcomas are rare and account for 0.04 % of all malignant breast tumors.</p>
</abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>Breast</kwd>
<kwd>Primary angiosarcoma</kwd>
</kwd-group>
<custom-meta-group>
<custom-meta>
<meta-name>issue-copyright-statement</meta-name>
<meta-value>© Indian Association of Surgical Oncology 2014</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
</pmc>
</record>

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