Delk Victoria D, Pasham Vishwajeeth, McKinnon Kathleen, Shah Pranav
Internal Medicine, Medical University of South Carolina, Charleston, USA.
Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, USA.
Cureus. 2025 Jun 20;17(6):e86409. doi: 10.7759/cureus.86409. eCollection 2025 Jun.
Staphylococcal infections remain a prominent cause of hospital- and community-acquired infections in the United States. Glomerulonephritis with predominant Immunoglobulin A (IgA) deposition following staphylococcal infection has been described as IgA-dominant postinfectious glomerulonephritis (IgA-PIGN). This clinical entity can mimic Henoch-Schönlein purpura nephritis (HSPN) given that it may also be preceded by staphylococcal infection, have similar kidney biopsy findings, and present with similar signs and symptoms. Our patient presented with a palpable purpuric rash and acute kidney injury following methicillin-sensitive (MSSA) bacteremia treated with intravenous cefazolin. A skin biopsy revealed leukocytoclastic vasculitis and vascular IgA deposition. Urinalysis showed active urinary sediment with hematuria and proteinuria. These findings were concerning for possible HSPN that was triggered by either staphylococcal infection or antibiotic exposure. Given worsening renal injury, the patient was started on empiric methylprednisone while awaiting kidney biopsy. When performed, the findings of diffuse proliferative glomerulonephritis with exudative features, subepithelial and mesangial deposits with strong C3 and moderate IgA staining were more consistent with IgA-PIGN over HSPN. Since IgA-PIGN is not responsive to steroids and may in fact be worsened by immunosuppression, methylprednisone was discontinued. The patient's renal function improved; however, he developed multi-organism bacteremia and duodenal perforation, ultimately leading to death. This case demonstrates the importance of distinguishing IgA-PIGN from HSPN in a patient with Staphylococcal infection presenting with renal injury and purpuric rash. Characteristic clinical signs and renal biopsy findings may aid in differentiating the two clinical entities so that the appropriate treatment can be initiated.
在美国,葡萄球菌感染仍是医院获得性感染和社区获得性感染的主要原因。葡萄球菌感染后以免疫球蛋白A(IgA)沉积为主的肾小球肾炎被描述为IgA主导的感染后肾小球肾炎(IgA-PIGN)。鉴于该临床实体也可能先有葡萄球菌感染,具有相似的肾活检结果,并表现出相似的体征和症状,故可模仿过敏性紫癜肾炎(HSPN)。我们的患者在接受静脉注射头孢唑林治疗甲氧西林敏感(MSSA)菌血症后出现可触及的紫癜性皮疹和急性肾损伤。皮肤活检显示白细胞破碎性血管炎和血管IgA沉积。尿液分析显示有血尿和蛋白尿的活动性尿沉渣。这些发现提示可能是由葡萄球菌感染或抗生素暴露引发的HSPN。鉴于肾损伤加重,患者在等待肾活检期间开始经验性使用甲基泼尼松。肾活检结果显示,具有渗出性特征的弥漫性增生性肾小球肾炎、上皮下和系膜沉积物,C3染色强而IgA染色中等,这些结果更符合IgA-PIGN而非HSPN。由于IgA-PIGN对类固醇无反应,实际上免疫抑制可能会使其恶化,因此停用了甲基泼尼松。患者的肾功能有所改善;然而,他发生了多种微生物菌血症和十二指肠穿孔,最终导致死亡。该病例表明,在患有肾损伤和紫癜性皮疹的葡萄球菌感染患者中,区分IgA-PIGN和HSPN的重要性。特征性的临床体征和肾活检结果可能有助于区分这两种临床实体,从而启动适当的治疗。