An Atypical Case of Anti GBM Disease

Sabrina Shahrin, Allahverdi Mahmud, Babrul Alam
{"title":"An Atypical Case of Anti GBM Disease","authors":"Sabrina Shahrin, Allahverdi Mahmud, Babrul Alam","doi":"10.3329/bjm.v34i20.66181","DOIUrl":null,"url":null,"abstract":"Anti GBM disease is a very rare type of small vessel vasculitis. The incidence is around less than 1 per million per year .This disease is also known as “Good Pasteur Disease”. Usually it presents with rapidly progressive glomerulonephritis with or without lung haemorrhage. The pathognomonic hallmark of the disease is strong linear IgG deposition along the GBM along with positive anti GBM antibody. But when the circulating antibody is absent in the blood, with mild renal impairment it is termed as atypical anti GBM disease. Recently we have found a 26 years old gentleman who presented with leg swelling for 1.5 months along with decreased urine output. He was non diabetic, normotensive, there was no history of joint pain, rash, no offending medication intake, or coughing out of blood. His urine R/E report showed Alb+++, RBC-plenty. After admission his serum creatinine was increasing rapidly. We have done renal biopsy and started treatment with I/V methylprednisolone followed by oral steroid. He had nephrotic range proteinuria. His auto antibody profile and HBsAg, Anti HCV was negative. We have done renal biopsy and it showed crescentic GN with strong linear deposition of IgG. His anti GBM Ab was negative. Thus we labelled the case as atypical anti GBM disease. Now patient is on RRT and we started therapeutic plasma exchange.\nJ Medicine 2023; Vol. 34, No. 2(1) Supplement: 220","PeriodicalId":8721,"journal":{"name":"Bangladesh Journal of Veterinary Medicine","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bangladesh Journal of Veterinary Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/bjm.v34i20.66181","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

Anti GBM disease is a very rare type of small vessel vasculitis. The incidence is around less than 1 per million per year .This disease is also known as “Good Pasteur Disease”. Usually it presents with rapidly progressive glomerulonephritis with or without lung haemorrhage. The pathognomonic hallmark of the disease is strong linear IgG deposition along the GBM along with positive anti GBM antibody. But when the circulating antibody is absent in the blood, with mild renal impairment it is termed as atypical anti GBM disease. Recently we have found a 26 years old gentleman who presented with leg swelling for 1.5 months along with decreased urine output. He was non diabetic, normotensive, there was no history of joint pain, rash, no offending medication intake, or coughing out of blood. His urine R/E report showed Alb+++, RBC-plenty. After admission his serum creatinine was increasing rapidly. We have done renal biopsy and started treatment with I/V methylprednisolone followed by oral steroid. He had nephrotic range proteinuria. His auto antibody profile and HBsAg, Anti HCV was negative. We have done renal biopsy and it showed crescentic GN with strong linear deposition of IgG. His anti GBM Ab was negative. Thus we labelled the case as atypical anti GBM disease. Now patient is on RRT and we started therapeutic plasma exchange. J Medicine 2023; Vol. 34, No. 2(1) Supplement: 220
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
抗GBM疾病的非典型病例
抗GBM疾病是一种非常罕见的小血管炎。每年的发病率不到百万分之一,这种疾病也被称为“良性巴斯德病”。通常表现为快速进展的肾小球肾炎伴或不伴肺出血。该病的病理特征是沿GBM呈强线性IgG沉积,并伴有抗GBM抗体阳性。但当血液中缺乏循环抗体,伴有轻度肾功能损害时,称为非典型抗GBM病。最近,我们发现了一位26岁的男士,他的腿肿胀了1.5个月,同时尿量减少。患者无糖尿病,血压正常,无关节痛、皮疹病史,无不良用药史,无咳血史。他的尿液R/E报告显示alb++,红细胞充足。入院后血清肌酐迅速升高。我们已经做了肾活检,并开始用I/V甲基强的松龙治疗,然后口服类固醇。他患有肾病范围蛋白尿。自身抗体及HBsAg、Anti - HCV均为阴性。我们做了肾活检,发现月牙形肾小球,并有很强的IgG线状沉积。他的抗GBM抗体呈阴性。因此,我们将该病例标记为非典型抗GBM疾病。现在病人正在接受RRT治疗,我们开始了治疗性血浆交换。中华医学杂志2023;第34卷,第2(1)号补编:220
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Prevalence, duration of illness, and mortality of lumpy skin disease at Chuadanga Sadar Upazila, Bangladesh Evaluation of relative efficiency of oocyte collection techniques from abattoir-derived goat ovaries Constraints and recommendation for countrywide extension of artificial insemination in buffalo, goat and sheep Conception rates of cows inseminated with frozen semen of Rural Development Academy, Bogura, Bangladesh Welfare assessment of dairy cows in commercial farms in Chattogram, Bangladesh
×
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