Abstract
The terms membranoproliferative glomerulonephritis (MPGN) and mesangiocapillary glomerulonephritis (MCGN) are interchangeable and refer to the light microscopic appearances of cellular proliferation in the mesangial regions of the glomeruli, with expansion of both cells and mesangial matrix, accompanied by thickening of the glomerular capillary walls. Rather than being a specific disease, MPGN is a morphological pattern which is associated with a wide range of distinct (and usually systemic) diseases. Recent developments in the understanding of these conditions emphasise the importance of establishing underlying disorder.
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Notes
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Complement haemolytic activity: patient serum across a range of dilutions is used to lyse antibody-coated sheep erythrocytes. Lack of haemolysis at a given dilution suggests deficiency of complement component(s).
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Sethi S, Fervenza FC. Membranoproliferative glomerulonephritis: pathogenetic heterogeneity and proposal for a new classification. Semin Nephrol. 2011;31(4):341–8.
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Gale, D.P., Owen-Casey, M. (2014). Membranoproliferative Glomerulonephritis and C3 Glomerulopathy. In: Harber, M. (eds) Practical Nephrology. Springer, London. https://doi.org/10.1007/978-1-4471-5547-8_18
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