Chamarthi Gajapathiraju, Clapp William L, Bejjanki Harini, Auerbach Jena, Koratala Abhilash
Nephrology/Renal Transplantation, University of Florida Health, Gainesville, USA.
Pathology, University of Florida Health, Gainesville, USA.
Cureus. 2020 Feb 28;12(2):e7127. doi: 10.7759/cureus.7127.
Infection-related glomerulonephritis (IRGN) is an immune complex-mediated glomerulonephritis (GN), often preceded by infection with subsequent recovery of renal function after the resolution of the infection. C3 deposition in the absence of immune complex deposits can be seen in patients with IRGN, but with the emergence of C3 glomerulonephritis (C3GN), the distinction is difficult as the clinical and pathological presentation may be similar. However, their treatment and clinical course vary significantly. A 64-year-old man with a history of hypertension and bioprosthetic aortic valve presented to the Emergency Department with left upper quadrant (LUQ) pain and a purpuric rash on bilateral lower extremities. The patient became septic, and further workup during the hospitalization revealed endocarditis secondary to Streptococcus viridans. On admission, the patient had acute kidney injury (AKI) with a serum creatinine of 3.79 mg/dl, which peaked at 5.72 mg/dl during the hospitalization. Renal biopsy demonstrated segmental necrotizing glomerulonephritis on light microscopy, predominant C3 deposition on immunofluorescence (IF) staining, and mesangial and paramesangial deposits on electron microscopy. This histologic picture can be seen both in IRGN and C3GN. The patient was treated with intravenous ceftriaxone for six weeks for endocarditis and the kidney injury was managed with supportive care. The patient's renal function improved and complement levels normalized, supporting the diagnosis of IRGN retrospectively. IRGN can mimic C3GN, and evaluation for alternate pathways of the complement system may be warranted in patients with atypical presentation of IRGN.
感染相关性肾小球肾炎(IRGN)是一种免疫复合物介导的肾小球肾炎(GN),通常在感染后发生,感染消退后肾功能随之恢复。IRGN患者可见无免疫复合物沉积时的C3沉积,但随着C3肾小球肾炎(C3GN)的出现,由于临床和病理表现可能相似,鉴别变得困难。然而,它们的治疗和临床病程差异很大。一名64岁男性,有高血压病史和生物人工主动脉瓣,因左上腹(LUQ)疼痛和双下肢紫癜性皮疹就诊于急诊科。患者发生败血症,住院期间进一步检查发现由草绿色链球菌引起的感染性心内膜炎。入院时,患者患有急性肾损伤(AKI),血清肌酐为3.79mg/dl,住院期间峰值达到5.72mg/dl。肾活检光镜显示节段性坏死性肾小球肾炎,免疫荧光(IF)染色主要为C3沉积,电镜显示系膜和系膜旁沉积。这种组织学表现可见于IRGN和C3GN。患者因感染性心内膜炎接受静脉注射头孢曲松治疗六周,肾损伤采用支持治疗。患者肾功能改善,补体水平恢复正常,回顾性支持IRGN的诊断。IRGN可模仿C3GN,对于IRGN非典型表现的患者,可能有必要评估补体系统的替代途径。