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dc.contributor.authorRojas-Jaimes, J.
dc.contributor.authorHugo Rojas Figueroa, V.
dc.contributor.authorCorcuera-Ciudad, R.
dc.contributor.authorArenas, J.
dc.contributor.authorGarcía-Reynoso, J.
dc.date.accessioned2025-10-31T18:33:44Z
dc.date.available2025-10-31T18:33:44Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/20.500.12805/5003
dc.description.abstractGranulomatosis with polyangiitis with nasal septal perforation can be confused with infectious diseases such as mucosal leishmaniasis, so these cases warrant an in-depth study in order to provide the correct treatment. Among the main characteristics to consider to define a Wegener's granulomatosis as opposed to an infectious disease are vasculitis, lymphadenopathy, and sinusopathy.en_US
dc.description.sponsorshipPublished with written consent of the patient. We thank the native speakers of the English language Illa Rocconi Quintanilla and Alejandro Basauri for the revision of the language of this manuscript.
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherJohn Wiley and Sons
dc.relation.ispartofurn:issn:2050-0904
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectSDG 3en_US
dc.subjectAutoimmune Diseases and Vasculitis Mechanismsen_US
dc.subjectANCA Associated Vasculitis Mechanisms and Treatmentsen_US
dc.titleWegener's granulomatosis and differential diagnosis of mucosal leishmaniasisen_US
dc.typehttps://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.doihttps://doi.org/10.1002/ccr3.4280
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.03.08
dc.type.otherResearch article
dc.identifier.journalClinical Case Reports
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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