An Unusual Case of Seronegative Cryoglobulinemic Glomerulonephritis with Dominant Organized IgA Deposits Associated with Staphylococcal Infection: Casual or Causal Relationship?

Glomerular diseases Pub Date : 2023-07-03 eCollection Date: 2023-01-01 DOI:10.1159/000531737
José C De La Flor Merino, Jacqueline Apaza, Francisco Díaz, Edna Sandoval, Francisco Valga, Daniel Villa, Alexander Marschall, María Luisa Abascal, Andrea Rivas, Michael Cieza
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Abstract

Introduction: Cryoglobulinemia refers to the presence of cryoglobulins (CGs) in the serum, encompassing a group of diseases caused by the type of circulating GC. Cryoglobulinemic glomerulonephritis (CryoGN) is the principal manifestation of renal involvement. The diagnosis may be challenging because the hallmark of cryoglobulinemia is the detection of CG in the serum. However, cases of CryoGN without serological evidence of CGs are not uncommon in clinical practice, often diagnosed by anatomopathological findings in the renal biopsy.

Case presentation: We report the case of an 86-year-old male who developed renal impairment, nephritic syndrome, and nephrotic-range proteinuria, without serological evidence of CGs, associated with staphylococcal bacteremia without apparent focus. Renal biopsy and pathological examination showed a membranoproliferative glomerulonephritis pattern with CD61-negative pseudothrombi. Immunofluorescence microscopy showed atypical IgA-dominant deposits. Electron microscopy revealed amorphous subendothelial and mesangial deposits and organized electrodense deposits within capillary loops (pseudothrombi) with microtubular substructure measuring 20-40 nm in thickness. These findings were consistent with seronegative CryoGN and microtubular organized atypical IgA-dominant deposits.

Discussion: In this report, we discuss the clinical, analytical, and histopathological findings of a rare case of CryoGN without serological evidence of CGs. Regarding the etiology that triggered the glomerular disease in our patient, we conducted an exhaustive study in order to determine the underlying cause of CryoGN. At the time of biopsy, the patient had an active staphylococcal bacteremia. There are reports that postulate that staphylococcal antigens drive activation of immune system and in consequence, could cause this rare form of IgA-dominant glomerulonephritis with cryoglobulinemic features. After ruling out other causes of cryoglobulinemia, we discuss a plausible causal relationship of the staphylococcal infection in the pathogenesis of CryoGN in our patient.

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一例罕见的血清阴性冷球蛋白血症肾小球肾炎,伴有与葡萄球菌感染相关的显性有组织IgA沉积:偶然关系还是因果关系?
简介:冷球蛋白血症是指血清中存在冷球蛋白(CG),包括一组由循环GC类型引起的疾病。冷球蛋白血症性肾小球肾炎(CryoGN)是肾脏受累的主要表现。诊断可能具有挑战性,因为冷球蛋白血症的标志是血清中CG的检测。然而,在临床实践中,没有CGs血清学证据的CryoGN病例并不罕见,通常通过肾活检中的解剖病理学发现来诊断。病例介绍:我们报告了一例86岁的男性,他出现了肾损伤、肾病综合征和肾病范围蛋白尿,没有CGs的血清学证据,与葡萄球菌菌血症相关,没有明显的病灶。肾活检和病理检查显示膜增殖性肾小球肾炎,CD61阴性假血栓。免疫荧光显微镜显示非典型IgA占优势的沉积物。电子显微镜显示无定形内皮下和系膜沉积以及毛细血管环内有组织的电沉积(假血栓),微管亚结构厚度为20-40nm。这些发现与血清阴性CryoGN和微管组织的非典型IgA优势沉积物一致。讨论:在本报告中,我们讨论了一例罕见的CryoGN病例的临床、分析和组织病理学结果,该病例没有CGs的血清学证据。关于引发我们患者肾小球疾病的病因,我们进行了一项详尽的研究,以确定CryoGN的根本原因。活检时,患者有活动性葡萄球菌菌血症。有报道认为,葡萄球菌抗原驱动免疫系统的激活,因此可能导致这种罕见的具有冷球蛋白血症特征的IgA显性肾小球肾炎。在排除了冷球蛋白血症的其他原因后,我们讨论了葡萄球菌感染在我们患者CryoGN发病机制中的可能因果关系。
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