Nodzynski Thomas, Sohani Zahra, Rajaram Ajay, Fiset Pierre Olivier, Bernard Chantal, Vasilevsky Murray, Weber Catherine
Division of Nephrology, McGill University, Montreal, QC, Canada.
Division of Infectious Diseases, McGill University, Montreal, QC, Canada.
Can J Kidney Health Dis. 2024 Dec 25;11:20543581241309977. doi: 10.1177/20543581241309977. eCollection 2024.
Infection-related glomerulonephritis (IRGN) is an immune-mediated glomerulonephritis caused by extra-renal infectious diseases. There has been an important shift in epidemiology in recent years, with a significant proportion of adults affected. The incidence of IRGN is higher amongst Indigenous populations and especially in those with multiple comorbidities. Beginning in 2019, we observed several IRGN cases amongst adult Indigenous peoples referred to the McGill University Health Center (MUHC). The aim of this article is to describe the demographic, clinical, and outcome data of these individuals and highlight the heterogeneity of IRGN in this population through 2 illustrative cases.
In total, 8 cases of IRGN were identified between 2019 and 2022. All patients presented with features of acute glomerulonephritis.
All patients had documented evidence of an infection that preceded their diagnosis of IRGN. IRGN was not the initial clinical diagnosis in all cases.
Half the patients received immunosuppression while the others received supportive care only.
Four patients required initiation of hemodialysis at time of presentation and at 2 years of follow-up, 3 of the 4 remained hemodialysis-dependent.
Our case series emphasizes the heterogenous clinical, laboratory, and pathological presentations that make the diagnosis of IRGN quite challenging. A high index of suspicion should be present when a patient presents with acute kidney injury, features of a glomerulonephritis, and an infection, especially those with multiple comorbidities and a preceding history of chronic kidney disease.
感染相关性肾小球肾炎(IRGN)是一种由肾外感染性疾病引起的免疫介导性肾小球肾炎。近年来流行病学发生了重要转变,相当一部分成年人受到影响。IRGN在原住民中的发病率较高,尤其是在那些患有多种合并症的人群中。从2019年开始,我们在转诊至麦吉尔大学健康中心(MUHC)的成年原住民中观察到几例IRGN病例。本文的目的是描述这些个体的人口统计学、临床和结局数据,并通过2个典型病例突出该人群中IRGN的异质性。
2019年至2022年间共确诊8例IRGN。所有患者均表现出急性肾小球肾炎的特征。
所有患者在诊断IRGN之前均有感染的记录证据。并非所有病例中IRGN都是最初的临床诊断。
一半患者接受免疫抑制治疗,而其他患者仅接受支持性治疗。
4例患者在就诊时需要开始血液透析,在2年的随访中,4例中有3例仍依赖血液透析。
我们的病例系列强调了异质性的临床、实验室和病理表现,这使得IRGN的诊断颇具挑战性。当患者出现急性肾损伤、肾小球肾炎特征和感染时,尤其是那些患有多种合并症和有慢性肾病既往史的患者,应保持高度的怀疑指数。