| Literature DB >> 23721509 |
Shintaro Mandai1, Makoto Aoyagi, Kiyotaka Nagahama, Yohei Arai, Suguru Hirasawa, Shota Aki, Naoto Inaba, Hiroyuki Tanaka, Yukio Tsuura, Teiichi Tamura, Sei Sasaki.
Abstract
A 37-year-old man developed Henoch--Schönlein purpura nephritis (HSPN) with nephrotic syndrome and rapidly progressive glomerulonephritis after otitis media and externa due to methicillin-resistant Staphylococcus aureus infection. Despite resolution of the infection and prednisolone therapy, his kidney disease worsened. However, the addition of cyclosporine A finally resulted in complete remission of the nephrotic syndrome. A review of similar cases with post-Staphylococcal infection HSPN revealed strong similarities between this entity and immunoglobulin A-dominant postinfectious glomerulonephritis (IgA-PIGN), an increasingly recognized form of PIGN typically associated with Staphylococcal infection, in both clinical and morphological features. Post-Staphylococcal infection HSPN may constitute a subgroup of IgA-PIGN.Entities:
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Year: 2013 PMID: 23721509 DOI: 10.3109/0886022X.2013.794703
Source DB: PubMed Journal: Ren Fail ISSN: 0886-022X Impact factor: 2.606