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Bilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant granulomatosis with polyangiitis: a case report

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dc.creatorVargas-Villanueva, Andrésspa
dc.creatorCarvajal-Saiz, Nataliaspa
dc.creatorMuñoz-Ortiz, Julianaspa
dc.creatorde-la-Torre, Alejandraspa
dc.date.accessioned2020-08-06T16:21:37Z
dc.date.available2020-08-06T16:21:37Z
dc.date.created2020-01-10spa
dc.description.abstractGranulomatosis with polyangiitis (GPA) (formerly known as Wegener´s granulomatosis) is a systemic necrotizing vasculitis belonging to a heterogeneous group of systemic anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis which affects small and medium-sized blood vessels [1, 2]. The annual incidence of GPA has been estimated to be 8 to 10 million, has a peak age of onset of 64 to 75 years [3], and the frequency of presentation in female and male individuals is similar. Constitutional signs like fever, asthenia, and weight loss are frequent (50%) but non-specific. Ear, nose, and throat signs (crusting rhinorrhea, sinusitis, chronic otitis, or damage of the facial cartilage) are present in 70 to 100% of cases at diagnosis [5]. Lung involvement, characterized by alveolar hemorrhage or parenchymatous nodules, affects 50 to 90% of patients [4]. The focal segmental necrotizing glomerulonephritis is the most frequent renal involvement in 40 to 100% of cases [6]. Involvement of the nervous system, the central nervous system, the pachymeninges, the heart, the pericardium, and the gastrointestinal system are less frequent, observed in a range of 5 to 40% of caseseng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1186/s12348-020-0195-6
dc.identifier.issnEISSN: 1869-5760
dc.identifier.urihttps://repository.urosario.edu.co/handle/10336/26413
dc.language.isoengspa
dc.publisherSpringer Naturespa
dc.relation.citationIssueNo. 2
dc.relation.citationTitleJournal of Ophthalmic Inflammation and Infection
dc.relation.citationVolumeVol. 10
dc.relation.ispartofJournal of Ophthalmic Inflammation and Infection, EISSN: 1869-5760, Vol.10, No.2 (2020); 6 pp.spa
dc.relation.urihttps://joii-journal.springeropen.com/track/pdf/10.1186/s12348-020-0195-6spa
dc.rights.accesRightsinfo:eu-repo/semantics/openAccess
dc.rights.accesoAbierto (Texto Completo)spa
dc.sourceJournal of Ophthalmic Inflammation and Infectionspa
dc.source.instnameinstname:Universidad del Rosario
dc.source.reponamereponame:Repositorio Institucional EdocUR
dc.subject.keywordCarboxymethylcellulosespa
dc.subject.keywordCyclophosphamidespa
dc.subject.keywordMethylprednisolonespa
dc.subject.keywordNeutrophil cytoplasmic antibodyspa
dc.subject.keywordQuinolonespa
dc.subject.keywordSteroidspa
dc.subject.keywordAdultspa
dc.subject.keywordBiomicroscopyspa
dc.subject.keywordCase reportspa
dc.subject.keywordClinical articlespa
dc.subject.keywordComputer assisted tomographyspa
dc.subject.keywordCornea edemaspa
dc.subject.keywordCornea perforationspa
dc.subject.keywordCornea ulcerspa
dc.titleBilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant granulomatosis with polyangiitis: a case reportspa
dc.title.TranslatedTitlePerforación corneal bilateral y prolapso del iris como complicación queratitis ulcerosa no periférica en un paciente con granulomatosis fulminante con poliangeítis: reporte de un casospa
dc.typearticleeng
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersion
dc.type.spaArtículospa
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