Rane Sharada, Mutyal Prerana, Dcunha Nicholas, Parkhi Mayur, Jadhav Meenal
Associate Professor, Department of Pathology, BJ Government Medical College, Pune, Maharashtra, India.
Junior Resident, Department of Pathology, BJ Government Medical College, Pune, Maharashtra, India.
J Clin Diagn Res. 2017 May;11(5):EC01-EC04. doi: 10.7860/JCDR/2017/25146.9795. Epub 2017 May 1.
Study of renal Immunofluorescence (IF) is an ancillary but essential technique in evaluation of renal biopsies in glomerulopathies and also it enlightens on the pathogenesis of nephrotic syndrome.
To determine the role of IF in evaluating definite subtyping and diagnosis of adult onset nephrotic syndrome and attempting clinicopathological correlation.
A total of 52 patients of adult onset nephrotic syndrome were evaluated clinically and with pertinent investigations; and subjected to USG guided percutaneous renal biopsy which was processed and stained for light microscopy and for immunofluorescence by direct method (DIF) using antibodies against IgG, IgM, IgA and C3.
The predominant age group affected was 18-47 years (78.85%). Male:female ratio was 1:0.63. The most frequent glomerular lesion encountered was Focal Segmental Glomerulosclerosis (FSGS, 36.54%) followed by lupus nephritis (26.92%) and IgA nephropathy (9.62%). The most common glomerular lesion in males was FSGS and that in females was lupus nephritis. DIF was mainly coarsely granular whenever present. One case of lupus nephritis and diabetic nephropathy, showed non specific IF. It was negative in all cases of FSGS, Minimal Change Disease (MCD) and renal amyloidosis. The IF helped in differentiating eight cases that were normal on light microscopy as IgA nephropathy (n=5) and authentic MCD (n=3). It helped in endorsing 19 cases of FSGS to be a progression of MCD. It was also of help in sub-typing all cases of Membranoproliferative Glomerulonephritis (MPGN) (n=3) as MPGN-Type I.
IF was of great help in diagnosing exact type of glomerulopathy in adult onset nephrotic syndrome and provided insight in its pathogenesis.
肾脏免疫荧光(IF)研究是评估肾小球疾病肾活检的一项辅助但必不可少的技术,它也有助于阐明肾病综合征的发病机制。
确定IF在评估成人起病型肾病综合征的明确亚型和诊断以及尝试进行临床病理相关性分析中的作用。
对52例成人起病型肾病综合征患者进行了临床评估和相关检查;并在超声引导下进行经皮肾活检,标本进行处理后用于光镜检查,并采用直接法(DIF)使用抗IgG、IgM、IgA和C3抗体进行免疫荧光染色。
受影响的主要年龄组为18 - 47岁(78.85%)。男女比例为1:0.63。最常见的肾小球病变是局灶节段性肾小球硬化(FSGS,36.54%),其次是狼疮性肾炎(26.92%)和IgA肾病(9.62%)。男性最常见的肾小球病变是FSGS,女性是狼疮性肾炎。DIF出现时主要为粗颗粒状。1例狼疮性肾炎和糖尿病肾病显示非特异性IF。在所有FSGS、微小病变病(MCD)和肾淀粉样变性病例中均为阴性。IF有助于将8例光镜检查正常的病例区分为IgA肾病(n = 5)和真性MCD(n = 3)。它有助于确认19例FSGS是MCD的进展。它也有助于将所有膜增生性肾小球肾炎(MPGN,n = 3)病例亚型分类为I型MPGN。
IF在诊断成人起病型肾病综合征的确切肾小球病类型方面有很大帮助,并为其发病机制提供了见解。