Abstract
Objective
To find out the incidence and natural history of IgMN in India.
Methods
Renal biopsies of children ≤12 y age of last 6 y were retrospectively evaluated. Their clinical and biochemical presentation were correlated. Patients with systemic diseases/disorders were excluded from the study.
Results
Immunoglobulin M nephropathy (IgMN) constituted 11.9% (n = 28) of 236 renal biopsies. Mean age was 10 y, predominant in boys (n = 24), most of the patients presented with proteinuria and edema. The most common associated histopathological finding was mesangial proliferative glomerulonephritis (MePGN) in 60.7% (n = 17) followed by minimal change disease (MCD) in 28.6% (n = 8) and focal segmental glomerulosclerosis (FSGS) in 10.7% (n = 3). In 85.7%, IgM appeared as the sole immunoglobulin deposit mainly in mesangial regions, followed by accompanied C3 in 3.6% (n = 1) and C1q + C3 in 10.7% (n = 3) biopsies.
Conclusions
IgMN was observed in 11.9% biopsies with commonest morphology of MePGN followed by MCD and FSGS; proteinuria was bad prognosticator in addition to FSGS and co-deposition of other immunoglobulins had no significance.
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Abbreviations
- FSGS:
-
Focal and Segmental Glomerulosclerosis
- IF:
-
Immunofluorescence
- IgMN:
-
IgM Nephropathy
- LM:
-
Light Microscopy
- MCD:
-
Minimal Change Disease
- MePGN:
-
Mesangial Proliferative Glomerulonephritis
- SCr:
-
Serum Creatinine
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Vanikar, A.V., Kanodia, K.V., Patel, R.D. et al. IgM Nephropathy in India: A Single Centre Experience. Indian J Pediatr 79, 1025–1027 (2012). https://doi.org/10.1007/s12098-012-0693-0
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DOI: https://doi.org/10.1007/s12098-012-0693-0