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dc.contributor.authorPimentel-Quiroz, V.R.
dc.contributor.authorUgarte-Gil, M.
dc.contributor.authorSumire-Umeres, J.
dc.contributor.authorPastor-Asurza, C.
dc.date.accessioned2025-10-31T18:32:41Z
dc.date.available2025-10-31T18:32:41Z
dc.date.issued2016
dc.identifier.urihttps://hdl.handle.net/20.500.12805/4742
dc.description.abstractGiant cell arteritis (GCA) is the most common primary vasculitis worldwide, affecting mainly older adult women. GCA affects medium- and large-size arteries, most commonly the extracranial branches of the carotid artery. The gold standard for the diagnosis of GCA is temporal artery biopsy; lesions may include fragmentation of the internal elastic lamina, multinucleated giant cells, and lymphohistiocytary adventitial infiltrate. Inflammation is focal and segmental ("skipped lesions"), which may lead to false-negative biopsy results. We wish to report a patient who we have diagnosed with possible GCA with coronary involvement and aortitis, whose disease debuted without classic symptoms...en_US
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofurn:issn:1076-1608
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.subject-en_US
dc.subject-en_US
dc.titleCoronary and Aortic Involvement as Initial Manifestations of Possible Giant Cell Arteritis in a Patient Without Cardiovascular Comorbiditiesen_US
dc.typehttps://purl.org/coar/resource_type/c_545b
dc.identifier.doihttps://doi.org/10.1097/RHU.0000000000000442
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.04
dc.type.otherLetter to the editor
dc.identifier.journalJournal of Clinical Rheumatology
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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