Lymphocytic myocarditis with suspected granulomatosis with polyangiitis presenting as cardiogenic shock, restrictive cardiomyopathy and complete heart block

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dc.contributor.authorAnderson, Wesley L.
dc.contributor.authorBahrami, Mubashir H.
dc.contributor.authorGuglin, Maya
dc.contributor.authorRao, Roopa
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2023-02-16T19:05:01Z
dc.date.available2023-02-16T19:05:01Z
dc.date.issued2021-02
dc.description.abstractWe report a case of restrictive cardiomyopathy from lymphocytic myocarditis in a patient with suspected granulomatosis with polyangiitis (GPA). The case was complicated by complete heart block and renal failure. The diagnosis was supported by upper airway involvement, elevated serum serine proteinase 3 antibodies, and endomyocardial biopsy with lymphocytic infiltration. The patient responded appropriately to aggressive immunosuppressive therapy.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationAnderson WL, Bahrami MH, Guglin M, Rao R. Lymphocytic myocarditis with suspected granulomatosis with polyangiitis presenting as cardiogenic shock, restrictive cardiomyopathy and complete heart block. J Cardiol Cases. 2021;24(3):102-105. Published 2021 Feb 26. doi:10.1016/j.jccase.2021.02.005en_US
dc.identifier.urihttps://hdl.handle.net/1805/31271
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.jccase.2021.02.005en_US
dc.relation.journalJournal of Cardiology Casesen_US
dc.sourcePMCen_US
dc.subjectAcute heart failureen_US
dc.subjectRestrictiveen_US
dc.subjectSystolic heart failureen_US
dc.subjectDiastolic heart failureen_US
dc.subjectAutoimmuneen_US
dc.titleLymphocytic myocarditis with suspected granulomatosis with polyangiitis presenting as cardiogenic shock, restrictive cardiomyopathy and complete heart blocken_US
dc.typeArticleen_US
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