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dc.contributor.authorHalperin, Den_US
dc.contributor.authorHallam, Sen_US
dc.contributor.authorHaroon, Aen_US
dc.contributor.authorButler, Ten_US
dc.contributor.authorAgrawal, Sen_US
dc.date.accessioned2017-03-24T15:01:53Z
dc.date.available2016-03-29en_US
dc.date.issued2016en_US
dc.date.submitted2017-01-18T22:42:14.312Z
dc.identifier.issn2090-6560en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/22219
dc.description.abstractWaldenstrom's macroglobulinaemia is the most commonly reported subtype of lymphoplasmacytic lymphoma (LPL); it is characterised by IgM secretion. Neurological complications are common usually as a result of hyperviscosity. In rare cases, cells can infiltrate the central nervous system; this is known as Bing-Neel syndrome. We report the case of a 57-year-old male with lymphoplasmacytic lymphoma of the IgG-subtype with neurological symptoms and the consequent finding of lymphoplasmacytoid cells in his cerebrospinal fluid as well as deposits on MRI and PET-CT imaging. This is the first report of Bing-Neel syndrome in IgG-subtype LPL. We discuss the biological and radiological markers of his disease, including PET imaging, which has been minimal in this area to date.en_US
dc.format.extent3931709 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofCase Rep Hematolen_US
dc.rightsCC-BY
dc.titleBing-Neel Syndrome Case Report: A Previously Undocumented IgG Variant with MRI, PET/CT, and PET/MRI Imaging.en_US
dc.typeArticle
dc.rights.holder© 2016 Daniel Halperin et al.
dc.identifier.doi10.1155/2016/3931709en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/27144041en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume2016en_US
dcterms.dateAccepted2016-03-29en_US


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