Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12564/584
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dc.contributor.authorŁysiak, Natalia-
dc.contributor.authorPodraza, Zofia-
dc.contributor.authorRóżańska, Maria-
dc.contributor.authorNiemczyk, Stanisław-
dc.date.accessioned2025-01-08T09:20:07Z-
dc.date.available2025-01-08T09:20:07Z-
dc.date.issued2024-
dc.identifier.citationPediatria i Medycyna Rodzinnapl
dc.identifier.issn1734-1531-
dc.identifier.urihttp://hdl.handle.net/20.500.12564/584-
dc.descriptionLicencja CC-BY-NC-NDpl
dc.description.abstractIntroduction: Rapidly progressive glomerulonephritis is a rare clinical condition characterised by rapid loss of renal function over a short period of time, nephritic syndrome, and crescents in renal biopsy. Pauci-immune rapidly progressive glomerulonephritis is usually associated with vasculitis, therefore skin, joints, lungs and nervous system may be involved. Numerous cases of pauci-immune rapidly progressive glomerulonephritis related with COVID-19 vaccines have been described in the literature, but there is little data on its occurrence after COVID-19 infection. Case description: We present a case of a 61-year-old female patient who was diagnosed with ANCA-negative pauci-immune rapidly progressive glomerulonephritis with nervous and respiratory system involvement within 5 months from COVID-19 infection. Conclusions: Pauci-immune rapidly progressive glomerulonephritis might be triggered by SARS-CoV-2 infection.pl
dc.language.isoenpl
dc.relation.ispartofseriesPediatr Med Rodz 2024; 20 (2): 257–260;10.15557/PiMR.2024.0039-
dc.subjectSARS-CoV-2pl
dc.subjectrapidly progressive glomerulonephritispl
dc.subjectpauci-immunepl
dc.subjectANCA antibody-positive vasculitis (AAV)pl
dc.titleANCA-negative pauci-immune rapidly progressive glomerulonephritis after COVID-19 – a case reportpl
dc.typeinfo:eu-repo/semantics/articlepl
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