Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence Findings

Introduction: Nephrotic syndrome is characterised by altered permselectivity of the glomerular filtration barrier which is a common chronic renal disorder in children. In children, it is characterised by oedema, hypoalbuminemia and proteinuria. Aim: To study the clinical profile of nephrotic sy...

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Main Authors: S Indupriya, Sridhar Yerram, Chakravarthula Anupama
Format: Article
Language:English
Published: JCDR Research and Publications Pvt. Ltd. 2019-07-01
Series: Indian Journal of Neonatal Medicine and Research
Subjects:
Online Access:http://www.ijnmr.net/articles/PDF/2256/42502_CE[Ra1]_F(SHU)_PF1(AG_SHU)_PFA(SHU)_PB(AG_SHU)_PN(SHU).pdf
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spelling doaj-43efa0c19fff43af89b8232d213f7da32020-11-25T03:00:29ZengJCDR Research and Publications Pvt. Ltd. Indian Journal of Neonatal Medicine and Research2277-85272455-68902019-07-0173PO20PO2610.7860/IJNMR/2019/42502.2256Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence FindingsS Indupriya0Sridhar Yerram1Chakravarthula Anupama2Assistant Professor, Department of Paediatrics, Suraksha Children’s Hospital, Hyderabad, Telangana, India.Consultant Pediatrician, Suraksha Children’s Hospital, Hyderabad, Telangana, India.Consultant Pediatrician, Suraksha Children’s Hospital, Hyderabad, Telangana, India.Introduction: Nephrotic syndrome is characterised by altered permselectivity of the glomerular filtration barrier which is a common chronic renal disorder in children. In children, it is characterised by oedema, hypoalbuminemia and proteinuria. Aim: To study the clinical profile of nephrotic syndrome in patients and also to study histopathological and immunofluorescence findings and correlation with clinical response to treatment. Materials and Methods: A prospective clinical study was undertaken to study the ‘Clinical Spectrum of Nephrotic Syndrome with special reference to Histopathology and Immunofluorescence. Children with nephrotic syndrome upto the age group of 18 years admitted in the Nephrology ward over a period of one year from January 2008 to December 2008 were included. All patients who met the criteria for nephrotic syndrome (proteinuria >40 mg/m2 /hr serum albumin <2.5 gm/dL, serum cholesterol >200 mg/dL) were eligible for the study. The results were analysed based on the clinical profile histopathology and immunoflorescence findings of the cases. Results: A total of 72 cases with Nephrotic syndrome were included in this study, gross haematuria was noticed in 9 cases (12.5%), hypertension was noticed in 21 cases (29.2% of children).Upper Respiratory Tract Infection (URTI) was seen in 34 cases (77.27%), Urinary Tract Infection (UTI) seen in 03 cases (06.81%), viral fever was seen in 9 cases (12.5%), peritonitis seen in 3 cases (4.2%) and it was seen as the precipitating causes for relapse. Hypertension was seen in 46 cases (63.6%) of steroid resistant group and 24 hour urine protein excretion was more in steroid resistant group. Renal biopsy was done in 29 out of 72 children (42.7%). Minimal change nephrotic syndrome was seen in 11 cases (37.9%) that underwent biopsy irrespective of the indication. Mesangio-proliferative nephrotic syndrome was the most common type in non minimal change nephrotic syndrome, 13 cases (45%) out of 18 cases of nonminimal change nephrotic syndrome (62%). Conclusion: Immunofluorescence is very important in diagnosing secondary nephrotic syndrome and plays a very important role where light microscopy alone cannot help in diagnosis such as IgA and IgM nephropathy, and Lupus nephritis. http://www.ijnmr.net/articles/PDF/2256/42502_CE[Ra1]_F(SHU)_PF1(AG_SHU)_PFA(SHU)_PB(AG_SHU)_PN(SHU).pdfhenoch-schonlein purpuraminimal change diseaseproteinuriasystemic lupus erythematosus
collection DOAJ
language English
format Article
sources DOAJ
author S Indupriya
Sridhar Yerram
Chakravarthula Anupama
spellingShingle S Indupriya
Sridhar Yerram
Chakravarthula Anupama
Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence Findings
Indian Journal of Neonatal Medicine and Research
henoch-schonlein purpura
minimal change disease
proteinuria
systemic lupus erythematosus
author_facet S Indupriya
Sridhar Yerram
Chakravarthula Anupama
author_sort S Indupriya
title Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence Findings
title_short Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence Findings
title_full Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence Findings
title_fullStr Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence Findings
title_full_unstemmed Clinical Spectrum of Nephrotic Syndrome and Correlation with Histopathology and Immunofluorescence Findings
title_sort clinical spectrum of nephrotic syndrome and correlation with histopathology and immunofluorescence findings
publisher JCDR Research and Publications Pvt. Ltd.
series Indian Journal of Neonatal Medicine and Research
issn 2277-8527
2455-6890
publishDate 2019-07-01
description Introduction: Nephrotic syndrome is characterised by altered permselectivity of the glomerular filtration barrier which is a common chronic renal disorder in children. In children, it is characterised by oedema, hypoalbuminemia and proteinuria. Aim: To study the clinical profile of nephrotic syndrome in patients and also to study histopathological and immunofluorescence findings and correlation with clinical response to treatment. Materials and Methods: A prospective clinical study was undertaken to study the ‘Clinical Spectrum of Nephrotic Syndrome with special reference to Histopathology and Immunofluorescence. Children with nephrotic syndrome upto the age group of 18 years admitted in the Nephrology ward over a period of one year from January 2008 to December 2008 were included. All patients who met the criteria for nephrotic syndrome (proteinuria >40 mg/m2 /hr serum albumin <2.5 gm/dL, serum cholesterol >200 mg/dL) were eligible for the study. The results were analysed based on the clinical profile histopathology and immunoflorescence findings of the cases. Results: A total of 72 cases with Nephrotic syndrome were included in this study, gross haematuria was noticed in 9 cases (12.5%), hypertension was noticed in 21 cases (29.2% of children).Upper Respiratory Tract Infection (URTI) was seen in 34 cases (77.27%), Urinary Tract Infection (UTI) seen in 03 cases (06.81%), viral fever was seen in 9 cases (12.5%), peritonitis seen in 3 cases (4.2%) and it was seen as the precipitating causes for relapse. Hypertension was seen in 46 cases (63.6%) of steroid resistant group and 24 hour urine protein excretion was more in steroid resistant group. Renal biopsy was done in 29 out of 72 children (42.7%). Minimal change nephrotic syndrome was seen in 11 cases (37.9%) that underwent biopsy irrespective of the indication. Mesangio-proliferative nephrotic syndrome was the most common type in non minimal change nephrotic syndrome, 13 cases (45%) out of 18 cases of nonminimal change nephrotic syndrome (62%). Conclusion: Immunofluorescence is very important in diagnosing secondary nephrotic syndrome and plays a very important role where light microscopy alone cannot help in diagnosis such as IgA and IgM nephropathy, and Lupus nephritis.
topic henoch-schonlein purpura
minimal change disease
proteinuria
systemic lupus erythematosus
url http://www.ijnmr.net/articles/PDF/2256/42502_CE[Ra1]_F(SHU)_PF1(AG_SHU)_PFA(SHU)_PB(AG_SHU)_PN(SHU).pdf
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