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dc.contributor.authorRiancho Zarrabeitia, Leyre
dc.contributor.authorPeiró Callizo, E.
dc.contributor.authorDrake Pérez, Marta 
dc.contributor.authorGarcía-Montesinos Perea, Belén 
dc.contributor.authorTerán Villagrá, Nuria 
dc.contributor.authorMartínez Taboada, Víctor Manuel 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2020-04-27T15:22:05Z
dc.date.available2020-04-27T15:22:05Z
dc.date.issued2019
dc.identifier.issn0303-464X
dc.identifier.urihttp://hdl.handle.net/10902/18499
dc.description.abstractWe report the case of a 15-year old girl who presented with a non-tender right upper eyelid swelling. Magnetic resonance confirmed the presence of an enlargement of the orbicular muscle with moderate contrast enhancement. Biopsy revealed the presence of necrotizing granulomatous vasculitis. Further studies ruled out systemic involvement. Thus, she was diagnosed with isolated granulomatosis with polyangiitis (GPA). Treatment with steroids and methotrexate was started. Due to the persistence of the lesion, rituximab (RTX) was added with excellent clinical and radiological response. This is, to the best of our knowledge, the first case of isolated orbital GPA treated with RTX in a pediatric patient.es_ES
dc.format.extent6 p.es_ES
dc.language.isoenges_ES
dc.publisherSociedade Portuguesa de Reumatologiaes_ES
dc.rights© Sociedade Portuguesa de Reumatologiaes_ES
dc.sourceActa Reumatol Port 2019 Jul 8;44(Jul-Sep (3)):258-263es_ES
dc.subject.otherPediatrices_ES
dc.subject.otherANCA-Associated Vasculitises_ES
dc.subject.otherOrbital Inflammatory Diseasees_ES
dc.titleGranulomatosis with polyangiitis with isolated orbital involvement in children: a case report successfully treated with rituximab and review of the literaturees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.type.versionpublishedVersiones_ES


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