Renal biopsy in systemic infections: expect the unexpected.

IF 1.1 4区 医学 Q4 MICROSCOPY Ultrastructural Pathology Pub Date : 2023-01-02 DOI:10.1080/01913123.2022.2164099
Bangchen Wang, Alexandra Grand, Micah Schub, Harpreet Singh, David I Ortiz Melo, David N Howell
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Abstract

Infection-related glomerulonephritis is well recognized in patients with ongoing infections. It can be missed, however, if the infection is unusual or undetected. We present three cases where the renal biopsy findings prompted the identification or treatment of systemic infections.Case 1: A 84-year-old male presented with acute kidney injury (AKI) and IgA vasculitis on skin biopsy. A renal biopsy showed active glomerulonephritis with abundant neutrophils and predominantly mesangial immune complex deposits containing IgA. The findings prompted an infectious workup which was positive for COVID-19, suggesting exacerbation of IgA nephropathy by recent COVID-19 infection. Case 2: A 31-year-old female status post kidney transplant for granulomatosis with polyangiitis (GPA) had recent pregnancy with preterm delivery, disseminated herpes simplex virus (HSV) infection with HSV hepatitis, E. coli on urine culture, and AKI. A renal biopsy showed proliferative glomerulonephritis with subendothelial and mesangial immune complex deposits containing IgG and C3. The findings were most consistent with infection-related immune complex glomerulonephritis, most likely HSV-related. Case 3: A 78-year-old female presented with AKI, proteinuria, hematuria, and positive p-ANCA. Clinically, ANCA vasculitis was suspected, and renal biopsy did show focal, segmental, necrotizing glomerulonephritis. However, immunofluorescence and electron microscopy showed IgM-rich deposits in the mesangium. The unusual presentation prompted an infectious workup including a Bartonella antibody panel which showed very high titers, suggesting Bartonella endocarditis.Infection-related glomerulonephritis has a wide variety of presentations histologically and clinically. The three cases we present here emphasize the importance of recognizing these entities to help guide treatment and improve patient care.

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全身性感染的肾活检:预料意料之外。
感染相关性肾小球肾炎在持续感染的患者中是公认的。然而,如果感染不寻常或未被发现,它可能会被遗漏。我们提出三个病例,其中肾活检结果提示识别或治疗全身性感染。病例1:84岁男性,皮肤活检表现为急性肾损伤(AKI)和IgA血管炎。肾活检显示活动性肾小球肾炎伴大量中性粒细胞,主要是含有IgA的系膜免疫复合物沉积。这些发现促使进行了COVID-19阳性的感染性检查,表明最近的COVID-19感染加剧了IgA肾病。病例2:31岁女性,因肉芽肿合并多血管炎(GPA)肾移植术后,近期妊娠伴早产,播散性单纯疱疹病毒(HSV)感染伴HSV肝炎,尿培养大肠杆菌,AKI。肾活检显示增生性肾小球肾炎伴内皮下和系膜免疫复合物沉积,含有IgG和C3。这些发现与感染相关的免疫复合物肾小球肾炎最一致,最可能与单纯疱疹病毒相关。病例3:一名78岁女性,表现为AKI、蛋白尿、血尿和p-ANCA阳性。临床上,怀疑ANCA血管炎,肾活检确实显示局灶性,节段性,坏死性肾小球肾炎。然而,免疫荧光和电镜显示在系膜中有富含igm的沉积物。这种不寻常的表现促使感染性检查,包括巴尔通体抗体小组,显示非常高的滴度,提示巴尔通体心内膜炎。感染相关性肾小球肾炎具有多种组织学和临床表现。我们在这里提出的三个案例强调了认识这些实体的重要性,以帮助指导治疗和改善患者护理。
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来源期刊
Ultrastructural Pathology
Ultrastructural Pathology 医学-病理学
CiteScore
2.00
自引率
10.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: Ultrastructural Pathology is the official journal of the Society for Ultrastructural Pathology. Published bimonthly, we are the only journal to be devoted entirely to diagnostic ultrastructural pathology. Ultrastructural Pathology is the ideal journal to publish high-quality research on the following topics: Advances in the uses of electron microscopic and immunohistochemical techniques Correlations of ultrastructural data with light microscopy, histochemistry, immunohistochemistry, biochemistry, cell and tissue culturing, and electron probe analysis Important new, investigative, clinical, and diagnostic EM methods.
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