Show simple item record

dc.contributor.authorSadreddini, S
dc.contributor.authorNoshad, H
dc.contributor.authorMolaeefard, M
dc.contributor.authorNoshad, R
dc.date.accessioned2018-08-26T08:27:57Z
dc.date.available2018-08-26T08:27:57Z
dc.date.issued2008
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51333
dc.description.abstractBehcet'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 Behcet'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 Behcet'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.subjectRituximab
dc.subjectBehcet's disease
dc.subjectRetinal vasculitis
dc.titleTreatment of retinal vasculitis in Behcet's disease with rituximab
dc.typeArticle
dc.citation.volume18
dc.citation.issue3
dc.citation.spage306
dc.citation.epage308
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1007/s10165-008-0057-9


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record