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dc.contributor.authorSrivastava, Sen_US
dc.contributor.authorRajakariar, Ren_US
dc.contributor.authorAshman, Nen_US
dc.contributor.authorRaftery, Men_US
dc.contributor.authorBrown, Hen_US
dc.contributor.authorMartin, JEen_US
dc.date.accessioned2018-08-02T10:24:18Z
dc.date.available2011-09-06en_US
dc.date.issued2012-02en_US
dc.date.submitted2018-07-20T09:36:15.580Z
dc.identifier.issn2048-8505en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/42903
dc.description.abstractSarcoidosis is a multisystemic, granulomatous disease of unknown aetiology, which commonly involves the lungs, skin and the eyes. Renal sarcoidosis is rare. Recurrent renal sarcoidosis leading to transplant graft failure in adults has not been reported. We report a single case of steroid-resistant sarcoid with recurrence in a renal transplant and the central nervous system that was managed with infliximab. We describe successful resolution of granulomas in the transplant kidney and stabilization of renal function with catastrophic central nervous system recurrence upon withdrawal of infliximab.en_US
dc.format.extent53 - 55en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofClin Kidney Jen_US
dc.rightsCC-BY-NC
dc.titleInfliximab as long-term maintenance in steroid-resistant and recurrent sarcoidosis in a renal transplant with central nervous system involvement.en_US
dc.typeArticle
dc.rights.holder© 2012, Oxford University Press
dc.identifier.doi10.1093/ndtplus/sfr142en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/26069750en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume5en_US
dcterms.dateAccepted2011-09-06en_US


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