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									<identifier>oai:www.peertechzpublications.org:10.17352/2455-8591.000009</identifier>
									<datestamp>2016-10-06</datestamp>
									<setSpec>PTZ.IJICR:VOL2</setSpec>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										A Synchronous Presentation of AITL with Adenocarcinoma of Lung
										</dc:title><dc:creator>Kanagaraja Karunakaran Parathan</dc:creator><dc:description>&lt;p&gt;Angioimmunoblastic T-cell lymphoma (AITL) is a frequent subtype of peripheral T – cell lymphoma (PTCL) characterized by generalized lymphadenopathy, hepatosplenomegaly, and frequent B - symptoms. Extranodal manifestations are quite common in this subtype of Non Hodgkins Lymphoma which is characterized by frequent skin involvement. However, the extranodal disease should be evaluated thoroughly and a tissue diagnosis must be obtained to confirm lymphomatous involvement when the presentation is not classical. Here we report a case of AITL who presented with lung mass suspected to be due to lymphomatous involvement, but turned out to be a synchronous presentation of an adenocarcinoma of the lung. The possible relation between the two conditions is also elucidated.&lt;/p&gt;</dc:description>
										<dc:publisher>International Journal of Immunotherapy and Cancer Research - Peertechz Publications</dc:publisher>
										<dc:date>2016-10-06</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/2455-8591.000009</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Kanagaraja Karunakaran Parathan et al.</dc:rights>
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