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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Immunoblastic lymphadenopathy--report of a case.</title><author><name sortKey="Joshi, K" sort="Joshi, K" uniqKey="Joshi K" first="K." last="Joshi">K. Joshi</name></author><author><name sortKey="Shrinivasa, R" sort="Shrinivasa, R" uniqKey="Shrinivasa R" first="R." last="Shrinivasa">R. Shrinivasa</name></author><author><name sortKey="Shankar, S K" sort="Shankar, S K" uniqKey="Shankar S" first="S. K." last="Shankar">S. K. Shankar</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">740591</idno><idno type="pmc">2425083</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2425083</idno><idno type="RBID">PMC:2425083</idno><date when="1978">1978</date><idno type="wicri:Area/Pmc/Corpus">001978</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001978</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Immunoblastic lymphadenopathy--report of a case.</title><author><name sortKey="Joshi, K" sort="Joshi, K" uniqKey="Joshi K" first="K." last="Joshi">K. Joshi</name></author><author><name sortKey="Shrinivasa, R" sort="Shrinivasa, R" uniqKey="Shrinivasa R" first="R." last="Shrinivasa">R. Shrinivasa</name></author><author><name sortKey="Shankar, S K" sort="Shankar, S K" uniqKey="Shankar S" first="S. K." last="Shankar">S. K. Shankar</name></author></analytic><series><title level="j">Postgraduate Medical Journal</title><idno type="ISSN">0032-5473</idno><idno type="eISSN">1469-0756</idno><imprint><date when="1978">1978</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>A case of immunoblastic lymphadenopathy has been presented which had the characteristic clinical and histological features. The patient did not respond to chemotherapy and succumbed to the disease. Instead of the usual polyclonal gammopathy associated with this condition, he showed a fall in IgM levels, IgG and IgA being within normal limits. The significance of the latter finding is not known.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><label>Fig. 1</label><graphic xlink:href="postmedj00262-0035-a" xlink:role="673"></graphic></fig><fig id="F2"><label>Fig. 2</label><graphic xlink:href="postmedj00262-0035-b" xlink:role="673"></graphic></fig><fig id="F3"><label>Fig. 3</label><graphic xlink:href="postmedj00262-0036-a" xlink:role="674"></graphic></fig></sec></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Postgrad Med J</journal-id><journal-id journal-id-type="pmc">postmedj</journal-id><journal-title>Postgraduate Medical Journal</journal-title><issn pub-type="ppub">0032-5473</issn><issn pub-type="epub">1469-0756</issn><publisher><publisher-name>BMJ Group</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">740591</article-id><article-id pub-id-type="pmc">2425083</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Immunoblastic lymphadenopathy--report of a case.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Joshi</surname><given-names>K.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Shrinivasa</surname><given-names>R.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Shankar</surname><given-names>S. K.</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><month>10</month><year>1978</year></pub-date><volume>54</volume><issue>636</issue><fpage>672</fpage><lpage>675</lpage><abstract><p>A case of immunoblastic lymphadenopathy has been presented which had the characteristic clinical and histological features. The patient did not respond to chemotherapy and succumbed to the disease. Instead of the usual polyclonal gammopathy associated with this condition, he showed a fall in IgM levels, IgG and IgA being within normal limits. The significance of the latter finding is not known.</p><sec sec-type="scanned-figures"><title>Images</title><fig id="F1"><label>Fig. 1</label><graphic xlink:href="postmedj00262-0035-a" xlink:role="673"></graphic></fig><fig id="F2"><label>Fig. 2</label><graphic xlink:href="postmedj00262-0035-b" xlink:role="673"></graphic></fig><fig id="F3"><label>Fig. 3</label><graphic xlink:href="postmedj00262-0036-a" xlink:role="674"></graphic></fig></sec></abstract></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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