Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/34377
DC FieldValueLanguage
dc.contributor.authorGuchev, Filipen_US
dc.contributor.authorBojadjioska, Majaen_US
dc.contributor.authorVidinikj, Sonjaen_US
dc.contributor.authorSandevska, Emilijaen_US
dc.contributor.authorPetrova, Sanjaen_US
dc.contributor.authorAntova, Dubravkaen_US
dc.contributor.authorVasilevska, Anaen_US
dc.contributor.authorVejseli, Ronen_US
dc.date.accessioned2025-11-24T08:06:14Z-
dc.date.available2025-11-24T08:06:14Z-
dc.date.issued2025-01-
dc.identifier.issn1857-9345-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/34377-
dc.description.abstractGranulomatosis with polyangiitis, formerly known as Wegener's granulomatosis, is a condition often presenting with granulomatous vasculitis of both the upper and lower respiratory tracts together with glomerulonephritis. Here we present a case of a 17-year-old female patient, who presented with symptoms of pansinusitis with other symptoms gradually following. She was treated with cyclophosphamide which was later switched to rituximab and is now in remission.en_US
dc.language.isoenen_US
dc.publisherMacedonian Academy of Sciences and Arts/Walter de Gruyter GmbHen_US
dc.relation.ispartofPrilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)en_US
dc.subjectcyclophosphamideen_US
dc.subjectgranulomatosis polyangiitisen_US
dc.subjectpansinusitisen_US
dc.subjectrituximaben_US
dc.subjectvasculitisen_US
dc.titleA complicated case of granulomatosis with polyangiitisen_US
dc.typeArticleen_US
dc.identifier.doi10.2478/prilozi-2025-0005-
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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