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dc.contributor.authorSadreddini, S
dc.contributor.authorNoshad, H
dc.contributor.authorMolaeefard, M
dc.contributor.authorNoshad, R
dc.date.accessioned2018-08-26T06:33:19Z
dc.date.available2018-08-26T06:33:19Z
dc.date.issued2008
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/43680
dc.description.abstractBehأ§et's disease (BD) is more common in eastern than western countries. Physicians have frequently encountered problems in its treatment, especially eye involvement. Recurrent oral and genital aphthous ulcerations are the hallmarks of Behأ§et's disease but other organs can be involved and ocular disease is one of the most disabling manifestations. Up to now, there are some problems in treatment of the retinal vasculitis due to Behأ§et's disease. We reported one patient, with visual loss due to retinal vasculitis that was resistant to prednisolone and azathioprine. Our patient was treated successfully with rituximab and his remission was sustained for 24 months of follow-up. Rituximab is a chimeric monoclonal antibody that acts against the specific B cell antigen, CD20. The recent success of rituximab in autoimmune diseases, which is considered to be T cell-mediated, indicates that B cells must have a much broader role in the pathogenesis of autoimmune diseases than generally appreciated.
dc.language.isoEnglish
dc.relation.ispartofModern rheumatology
dc.subjectAdult
dc.subjectAntibodies, Monoclonal
dc.subjectAntibodies, Monoclonal, Murine-Derived
dc.subjectAntirheumatic Agents
dc.subjectBehcet Syndrome
dc.subjectHumans
dc.subjectMale
dc.subjectRemission Induction
dc.subjectRetinal Vasculitis
dc.subjectRituximab
dc.titleTreatment of retinal vasculitis in Behأ§et's disease with rituximab.
dc.typearticle
dc.citation.volume18
dc.citation.issue3
dc.citation.spage306
dc.citation.epage8
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1007/s10165-008-0057-9


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