Fibrillary Glomerulonephritis Diagnosis Is Enhanced by DNAJB9: Three Cases with Different Clinical, Anatomopathologic Features and Outcomes.

José C De La Flor, Marco Dominguez Davalos, Tania Linares Grávalos, Marina Alonso-Riaño, Francisco Díaz, Celia Rodríguez Tudero, Rocío Zamora González-Mariño, Michael Cieza Terrones, Jesús Hernández Vaquero
{"title":"Fibrillary Glomerulonephritis Diagnosis Is Enhanced by DNAJB9: Three Cases with Different Clinical, Anatomopathologic Features and Outcomes.","authors":"José C De La Flor, Marco Dominguez Davalos, Tania Linares Grávalos, Marina Alonso-Riaño, Francisco Díaz, Celia Rodríguez Tudero, Rocío Zamora González-Mariño, Michael Cieza Terrones, Jesús Hernández Vaquero","doi":"10.3390/pathophysiology32020022","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background:</b> Fibrillary glomerulonephritis (FGN) is a rare and poorly understood kidney disease characterized by the deposition of non-amyloid fibrils in the glomeruli. Its clinical heterogeneity and high rate of progression to end-stage renal disease (ESRD) pose significant diagnostic and therapeutic challenges. This case series aims to enhance awareness of FGN and emphasizes the need for further research to improve patient outcomes. <b>Case Reports:</b> We reviewed the clinical, histopathological, and therapeutic data of three patients with FGN diagnosed by kidney biopsy. The cases included variations in clinical presentation from nephrotic syndrome to rapidly progressive glomerulonephritis (RPGN). Diagnostic methods incorporated light microscopy, immunofluorescence, and electron microscopy, with the integration of DnaJ homolog subfamily B member 9 (DNAJB9) staining for confirmation. Patient 1 showed a more favorable response to rituximab, achieving complete remission (CR) at 6 months and maintaining CR after 3 years. Patient 2 showed only partial remission after 2 years following treatment with rituximab. Patient 3 presented with RPGN and rapidly progressed to ESRD despite aggressive immunosuppressive therapy. <b>Discussion:</b> DNAJB9 has emerged as both a specific and sensitive biomarker in patients with FGN and has facilitated accurate differentiation from other glomerulopathies. This series underscores the variability in clinical outcomes and responses to therapy as well as the importance of early and accurate diagnosis. <b>Conclusions</b>: FGN remains a diagnostic and therapeutic challenge due to its rarity and heterogeneity. Advances in biomarkers like DNAJB9 have improved diagnostic accuracy, distinguishing FGN from similar conditions such as immunotactoid glomerulopathy. Further research into pathophysiological mechanisms and targeted therapies is essential to optimize management and outcomes for affected patients.</p>","PeriodicalId":520741,"journal":{"name":"Pathophysiology : the official journal of the International Society for Pathophysiology","volume":"32 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12195910/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathophysiology : the official journal of the International Society for Pathophysiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/pathophysiology32020022","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Fibrillary glomerulonephritis (FGN) is a rare and poorly understood kidney disease characterized by the deposition of non-amyloid fibrils in the glomeruli. Its clinical heterogeneity and high rate of progression to end-stage renal disease (ESRD) pose significant diagnostic and therapeutic challenges. This case series aims to enhance awareness of FGN and emphasizes the need for further research to improve patient outcomes. Case Reports: We reviewed the clinical, histopathological, and therapeutic data of three patients with FGN diagnosed by kidney biopsy. The cases included variations in clinical presentation from nephrotic syndrome to rapidly progressive glomerulonephritis (RPGN). Diagnostic methods incorporated light microscopy, immunofluorescence, and electron microscopy, with the integration of DnaJ homolog subfamily B member 9 (DNAJB9) staining for confirmation. Patient 1 showed a more favorable response to rituximab, achieving complete remission (CR) at 6 months and maintaining CR after 3 years. Patient 2 showed only partial remission after 2 years following treatment with rituximab. Patient 3 presented with RPGN and rapidly progressed to ESRD despite aggressive immunosuppressive therapy. Discussion: DNAJB9 has emerged as both a specific and sensitive biomarker in patients with FGN and has facilitated accurate differentiation from other glomerulopathies. This series underscores the variability in clinical outcomes and responses to therapy as well as the importance of early and accurate diagnosis. Conclusions: FGN remains a diagnostic and therapeutic challenge due to its rarity and heterogeneity. Advances in biomarkers like DNAJB9 have improved diagnostic accuracy, distinguishing FGN from similar conditions such as immunotactoid glomerulopathy. Further research into pathophysiological mechanisms and targeted therapies is essential to optimize management and outcomes for affected patients.

DNAJB9增强对原纤维性肾小球肾炎的诊断:3例临床、解剖病理特征及预后不同的病例
背景:原纤维性肾小球肾炎(FGN)是一种罕见且知之甚少的肾脏疾病,其特征是肾小球内非淀粉样原纤维沉积。其临床异质性和高进展率终末期肾脏疾病(ESRD)提出了重大的诊断和治疗挑战。本病例系列旨在提高对FGN的认识,并强调进一步研究以改善患者预后的必要性。病例报告:我们回顾了3例肾活检诊断为FGN的患者的临床、组织病理学和治疗资料。这些病例包括从肾病综合征到快速进展性肾小球肾炎(RPGN)的临床表现变化。诊断方法包括光镜、免疫荧光和电镜,并整合DnaJ同源亚家族B成员9 (DNAJB9)染色进行确认。患者1对利妥昔单抗表现出更有利的反应,在6个月时达到完全缓解(CR),并在3年后保持CR。患者2在接受利妥昔单抗治疗2年后仅部分缓解。患者3表现为RPGN,尽管进行了积极的免疫抑制治疗,但仍迅速发展为ESRD。讨论:DNAJB9已成为FGN患者特异性和敏感性的生物标志物,并有助于与其他肾小球疾病的准确区分。这一系列强调了临床结果和治疗反应的可变性,以及早期和准确诊断的重要性。结论:由于其罕见性和异质性,FGN仍然是诊断和治疗的挑战。生物标志物如DNAJB9的进步提高了诊断的准确性,将FGN与类似的疾病(如免疫因子样肾小球病)区分开来。进一步研究病理生理机制和靶向治疗对于优化患者的治疗和预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信