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Clinico-pathologic spectrum of C3 glomerulopathy-an Indian experience
- Source :
- Diagnostic Pathology
- Publication Year :
- 2015
- Publisher :
- BioMed Central, 2015.
-
Abstract
- Background C3 glomerulopathy (C3GP) is characterized by deposition of complement C3 with absence/traces of immunoglobulins in the glomeruli and categorized into dense deposit disease (DDD), C3 glomerulonephritis (C3GN), complement factor H related protein 5(CFHR5) nephropathy etc. Collaborative efforts of pathologists, complement biologists and nephrologists worldwide are expanding the histomorphological pattern and laboratory findings related to C3GP. Hence, we studied point prevalence and morphological spectrum of C3GP in Indian patients to correlate morphological patterns with standard therapies and outcome of the patients. Methods Retrospective analysis of renal biopsies (2007-2012,n-4565), which on immunofluorescence (IF) had C3 dominant deposits with absence or trace amount of immunoglobulin was carried out. Histopathology and electronmicroscopy (EM) were reviewed; cases were re-classified as DDD and C3GN. Histomorphological patterns of both groups were compared and correlated with treatment. Clinical details and follow up of patients were retrieved from the department of nephrology. Results There were 31 cases (0.7%) of C3GP sub-classified as DDD (n-13) and C3GN (n-14). It was difficult to sub-classify 4 cases since EM showed overlapping features. C3GN and DDD had distinct clinical characteristics and disease outcome, though pathological features were overlapping. Majority of C3GP patients were males and were in 2nd to 4th decade of life. Nephrotic syndrome in DDD and nephritic-nephrotic presentation in C3GN patients was more common. Hypertension and oliguria were more often observed in C3GN than DDD. Membranoproliferative pattern (MPGN) was commonest pattern in DDD; other patterns seen were mesangial proliferative, mesangial expansive/nodular, exudative and crescentic. C3GN also had all the above patterns, the predominant ones being MPGN and mesangial proliferative. Limited follow-up revealed response to therapy only in C3GN (33%). Progression to ESRD was 33% in DDD and 10% cases in C3GN. Conclusion C3GP comprise 0.7% of all renal biopsies. MPGN pattern was the commonest morphological pattern in DDD whereas MPGN and mesangial proliferative pattern were equally dominant patterns in C3GN. EM of 4 cases (13%) showed intermediate features. Evaluation of alternate complement pathway must be done in all cases to identify the point of dysregulated alternate complement pathway and to confirm the diagnosis in ambiguous cases. Virtual slides The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1730070964135632
- Subjects :
- Male
Pathology
Nephrotic Syndrome
C3 Glomerulonephritis
Biopsy
Kidney Glomerulus
Fluorescent Antibody Technique
Nephrotic
Pilot Projects
Tertiary Care Centers
Glomerulonephritis
Prevalence
C3 glomerulopathy
Child
Dense deposit disease
General Medicine
Complement C3
Middle Aged
Treatment Outcome
Factor H
Disease Progression
Female
Adult
medicine.medical_specialty
Histology
Adolescent
Glomerulonephritis, Membranoproliferative
Complement
India
Alternate complement pathway
Pathology and Forensic Medicine
Nephropathy
Young Adult
Nephritic
Glomerulopathy
Predictive Value of Tests
medicine
Dense Deposit Disease
Humans
Retrospective Studies
business.industry
Research
medicine.disease
Microscopy, Electron
Kidney Failure, Chronic
business
CFHR5
Nephrotic syndrome
Biomarkers
Subjects
Details
- Language :
- English
- ISSN :
- 17461596
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Diagnostic Pathology
- Accession number :
- edsair.doi.dedup.....8feab555f703a753874fe24f311c9029