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dc.contributor.authorAydin F.
dc.contributor.authorSenturk N.
dc.contributor.authorYuksel E.
dc.contributor.authorYildiz L.
dc.contributor.authorCanturk T.
dc.contributor.authorTuranli A.
dc.date.accessioned2020-06-21T09:27:20Z
dc.date.available2020-06-21T09:27:20Z
dc.date.issued2007
dc.identifier.issn0019-5154
dc.identifier.urihttps://doi.org/10.4103/0019-5154.31928
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4008
dc.description.abstractPatients with lupus erythematous may develop an acute eruption clinically similar to toxic epidermal necrolysis or erythema multiforme. The presence of erythema multiforme-like lesions and characteristic pattern of immunological abnormalities including antinuclear antibody (speckled pattern), anti-Ro antibody or anti-La antibody and positive rheumatoid factor in lupus patients has been termed as Rowell's syndrome. Although diagnostic criteria of this syndrome have been reviewed recently, definite mechanisms of pathogenesis is still unknown. Here we reported a 29-year-old female patient who had systemic lupus erythematosus developed erythema multiforme-like lesions.en_US
dc.language.isoengen_US
dc.publisherMedknow Publications and Media Pvt. Ltden_US
dc.relation.isversionof10.4103/0019-5154.31928en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectErythema multiformeen_US
dc.subjectRowell's syndromeen_US
dc.subjectSystemic lupus erythematosusen_US
dc.titleSystemic lupus erythematosus with an erythema multiforme-like lesionsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume52en_US
dc.identifier.issue1en_US
dc.identifier.startpage56en_US
dc.identifier.endpage58en_US
dc.relation.journalIndian Journal of Dermatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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