隐性老虎:抗肾小球基底膜病的非典型表现

A. Lecamwasam, Darren Lee, A. Skene, L. McMahon
{"title":"隐性老虎:抗肾小球基底膜病的非典型表现","authors":"A. Lecamwasam, Darren Lee, A. Skene, L. McMahon","doi":"10.14740/WJNU173W","DOIUrl":null,"url":null,"abstract":"Anti-glomerular basement membrane (anti-GBM) disease is characterized by linear deposition of immunoglobulin G (IgG) along the GBM. The concurrence of anti-GBM disease with another type of glomerulonephritis has been well described. We report a case of necrotizing glomerulonephritis in association with prodromal systemic symptoms, deterioration in kidney function less rapid than expected, and the presence of circulating anti-GBM antibody. This was initially diagnosed histologically as immunoglobulin A (IgA) nephropathy based on immunohistochemistry (IHC) staining, but immunofluorescence (IF) staining on a subsequent biopsy was more consistent with a diagnosis of anti-GBM disease with co-existing mild IgA nephropathy. Prompt initiation of standard treatment of anti-GBM disease normalized kidney function. This case highlights that anti-GBM disease can present atypically and may also co-exist with another form of glomerulonephritis. World J Nephrol Urol. 2014;3(3):124-128 doi: http://dx.doi.org/10.14740/wjnu173w","PeriodicalId":91634,"journal":{"name":"World journal of nephrology and urology","volume":"3 1","pages":"124-128"},"PeriodicalIF":0.0000,"publicationDate":"2014-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hidden Tiger: An Atypical Presentation of Anti-Glomerular Basement Membrane Disease\",\"authors\":\"A. Lecamwasam, Darren Lee, A. Skene, L. McMahon\",\"doi\":\"10.14740/WJNU173W\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Anti-glomerular basement membrane (anti-GBM) disease is characterized by linear deposition of immunoglobulin G (IgG) along the GBM. The concurrence of anti-GBM disease with another type of glomerulonephritis has been well described. We report a case of necrotizing glomerulonephritis in association with prodromal systemic symptoms, deterioration in kidney function less rapid than expected, and the presence of circulating anti-GBM antibody. This was initially diagnosed histologically as immunoglobulin A (IgA) nephropathy based on immunohistochemistry (IHC) staining, but immunofluorescence (IF) staining on a subsequent biopsy was more consistent with a diagnosis of anti-GBM disease with co-existing mild IgA nephropathy. Prompt initiation of standard treatment of anti-GBM disease normalized kidney function. This case highlights that anti-GBM disease can present atypically and may also co-exist with another form of glomerulonephritis. World J Nephrol Urol. 2014;3(3):124-128 doi: http://dx.doi.org/10.14740/wjnu173w\",\"PeriodicalId\":91634,\"journal\":{\"name\":\"World journal of nephrology and urology\",\"volume\":\"3 1\",\"pages\":\"124-128\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"World journal of nephrology and urology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14740/WJNU173W\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"World journal of nephrology and urology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14740/WJNU173W","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

抗肾小球基底膜疾病的特征是免疫球蛋白G (IgG)沿肾小球基底膜呈线性沉积。抗gbm疾病与另一种类型的肾小球肾炎的并发已被很好地描述。我们报告一例坏死性肾小球肾炎,伴有前体全身性症状,肾功能恶化速度低于预期,并且存在循环抗gbm抗体。最初根据免疫组化(IHC)染色在组织学上诊断为免疫球蛋白A (IgA)肾病,但随后活检的免疫荧光(IF)染色更符合抗gbm疾病并共存轻度IgA肾病的诊断。及时开始标准治疗抗gbm疾病使肾功能正常化。本病例强调抗gbm疾病可以表现为非典型,也可能与另一种形式的肾小球肾炎共存。世界肾脏病杂志,2014;3(3):124-128 doi: http://dx.doi.org/10.14740/wjnu173w
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Hidden Tiger: An Atypical Presentation of Anti-Glomerular Basement Membrane Disease
Anti-glomerular basement membrane (anti-GBM) disease is characterized by linear deposition of immunoglobulin G (IgG) along the GBM. The concurrence of anti-GBM disease with another type of glomerulonephritis has been well described. We report a case of necrotizing glomerulonephritis in association with prodromal systemic symptoms, deterioration in kidney function less rapid than expected, and the presence of circulating anti-GBM antibody. This was initially diagnosed histologically as immunoglobulin A (IgA) nephropathy based on immunohistochemistry (IHC) staining, but immunofluorescence (IF) staining on a subsequent biopsy was more consistent with a diagnosis of anti-GBM disease with co-existing mild IgA nephropathy. Prompt initiation of standard treatment of anti-GBM disease normalized kidney function. This case highlights that anti-GBM disease can present atypically and may also co-exist with another form of glomerulonephritis. World J Nephrol Urol. 2014;3(3):124-128 doi: http://dx.doi.org/10.14740/wjnu173w
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Serum Cystatin C as an Index of Early Detection of Acute Kidney Injury in Children With Severe Malaria Clinical Utiliy of Routine Postoperative Laboratory Tests After Laparoscopic Prostate Surgery Do Levels of SARS-CoV-2 Anti-Spike Antibody Titers After Vaccination Predict Future Infections in Hemodialysis Patients? Albumin Loss in Post-Dilution On-Line Hemodiafiltration Compared With Pre-Dilution On-Line Hemodiafiltration and Conventional Hemodialysis Greens Mean Go: A Case Report Exploring a Vegetarian Diet in Chronic Kidney Disease
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1