{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,16]],"date-time":"2026-07-16T12:26:52Z","timestamp":1784204812594,"version":"3.55.0"},"reference-count":15,"publisher":"Oxford University Press (OUP)","issue":"9","license":[{"start":{"date-parts":[[2022,6,24]],"date-time":"2022-06-24T00:00:00Z","timestamp":1656028800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,9,29]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Staphylococcus-associated glomerulonephritis (GN) is an uncommon diagnosis in pediatric patients. Empiric therapy with steroids alone could potentially worsen the underlying infectious process in these patients, leading to worse clinical outcomes. An adolescent male diagnosed with GN was subsequently found to have chronic granulomatous disease with a Staphylococcus aureus liver abscess. His GN improved with antibiotics alone. This case illustrates the need to consider chronic infection, and primary immunodeficiency, in the differential diagnosis for new-onset GN.<\/jats:p>","DOI":"10.1093\/jpids\/piac057","type":"journal-article","created":{"date-parts":[[2022,6,24]],"date-time":"2022-06-24T07:06:17Z","timestamp":1656054377000},"page":"422-425","source":"Crossref","is-referenced-by-count":4,"title":["<i>Staphylococcus aureus<\/i>-Associated Glomerulonephritis and Chronic Granulomatous Disease in an Adolescent Male"],"prefix":"10.1093","volume":"11","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4057-862X","authenticated-orcid":false,"given":"Simon","family":"Parzen-Johnson","sequence":"first","affiliation":[{"name":"Division of Infectious Diseases, Ann & Robert H. Lurie Children\u2019s Hospital , Chicago, Illinois , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vidhi","family":"Dalal","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Ann & Robert H. Lurie Children\u2019s Hospital , Chicago, Illinois , USA"},{"name":"Northwestern University, Feinberg School of Medicine , Chicago, Illinois , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ravi","family":"Jhaveri","sequence":"additional","affiliation":[{"name":"Division of Infectious Diseases, Ann & Robert H. Lurie Children\u2019s Hospital , Chicago, Illinois , USA"},{"name":"Northwestern University, Feinberg School of Medicine , Chicago, Illinois , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2022,6,24]]},"reference":[{"key":"2022092906582400200_CIT0001","doi-asserted-by":"crossref","first-page":"S2","DOI":"10.1093\/jpids\/piy008","article-title":"Chronic granulomatous disease: epidemiology, pathophysiology, and genetic basis of disease","volume":"7","author":"Rider","year":"2018","journal-title":"J Pediatric Infect Dis Soc"},{"key":"2022092906582400200_CIT0002","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1186\/s13000-020-00980-6","article-title":"Clinicopathologic features of infection-related glomerulonephritis with IgA deposits: a French Nationwide study","volume":"15","author":"Miquelestorena-Standley","year":"2020","journal-title":"Diagn Pathol"},{"key":"2022092906582400200_CIT0003","doi-asserted-by":"crossref","first-page":"39","DOI":"10.2215\/CJN.05070516","article-title":"Staphylococcus infection-associated GN\u2014spectrum of IgA staining and prevalence of ANCA in a single-center cohort","volume":"12","author":"Satoskar","year":"2017","journal-title":"Clin J Am Soc Nephrol"},{"key":"2022092906582400200_CIT0004","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1136\/ard.62.5.388","article-title":"Antiphospholipid antibodies and infections","volume":"62","author":"Asherson","year":"2003","journal-title":"Ann Rheum Dis"},{"key":"2022092906582400200_CIT0005","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1007\/s13730-021-00586-x","article-title":"Rapidly progressive IgA vasculitis-associated nephritis successfully treated with immunosuppressive therapy in an adolescent with chronic granulomatous disease","volume":"10","author":"Tanaka","year":"2021","journal-title":"CEN Case Rep"},{"key":"2022092906582400200_CIT0006","first-page":"891","article-title":"Glomerulonephritis associated with chronic granulomatous disease and systemic lupus erythematosus","volume":"10","author":"Schmitt","year":"1995","journal-title":"Nephrol Dial Transplant"},{"key":"2022092906582400200_CIT0007","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1111\/j.0954-6820.1979.tb13502.x","article-title":"Immune complex glomerulonephritis in chronic granulomatous disease. 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