dc.creatorAppenzeller S.
dc.creatorDe Castro R.
dc.creatorDe Souza Queiroz L.
dc.creatorMadegan L.
dc.creatorSoledade C.
dc.creatorDe Araujo Zanardi V.
dc.creatorNucci A.
dc.creatorCendes F.
dc.creatorFernandes S.R.M.
dc.date2006
dc.date2015-06-30T18:11:48Z
dc.date2015-11-26T14:27:09Z
dc.date2015-06-30T18:11:48Z
dc.date2015-11-26T14:27:09Z
dc.date.accessioned2018-03-28T21:30:12Z
dc.date.available2018-03-28T21:30:12Z
dc.identifier
dc.identifierRheumatology International. , v. 26, n. 6, p. 577 - 580, 2006.
dc.identifier1728172
dc.identifier10.1007/s00296-005-0082-3
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-33645344105&partnerID=40&md5=5754c28e9ef6b8e64ef17f2467080c76
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/103446
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/103446
dc.identifier2-s2.0-33645344105
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1246250
dc.descriptionWe report a patient with longstanding Behçet disease who presented sudden onset of headache and facial paresis. The magnetic resonance imaging (MRI) showed a mass in the right thalamus, extending to the lentiform nucleus, subthalamic area, right cerebral peduncle and deep subcortical white matter. Stereotactic brain biopsy disclosed gliosis with no signs of malignancy. The diagnosis of a pseudotumoral form of neuro-Behçet disease was done and she was treated with pulse methylpredinisolone and intravenous cyclophosphamide. After 8 weeks she had improved and a new MRI showed disappearance of the tumor-like lesion. The differential diagnosis, especially with central nervous system tumor is emphasized. © Springer-Verlag 2005.
dc.description26
dc.description6
dc.description577
dc.description580
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dc.languageen
dc.publisher
dc.relationRheumatology International
dc.rightsfechado
dc.sourceScopus
dc.titleBrain Tumor-like Lesion In Behçet Disease
dc.typeArtículos de revistas


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