Abstract
Introduction: Idiopathic nodular glomerulosclerosis (ING) is a condition that has a vasculopathic glomerular histological pattern. Case presentation: The authors present the case of a 44-year-old Hispanic smoker female with hypertension and peripheral arterial disease who presented nephrotic syndrome for 2 weeks. The patient was diagnosed with ING by percutaneous renal biopsy results, which showed global nodular mesangial matrix expansion, with linear staining accentuation of glomerular and tubular basement membrane for Immunoglobulin G (IgG) and albumin on immunofluorescence. Conclusions: ING is a rare disease with a poor renal prognosis and wide diagnostic approach; we highlight the importance of analyzing every piece of detail together to reach a definitive diagnosis.
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Alvizures Solares, S. R., Ibarra-Sifuentes, H. R., Ramírez Ramírez, M. G., Arteaga Muller, G. Y., & Valdez, J. C. (2020). Idiopathic nodular glomerulosclerosis and differential diagnosis. Brazilian Journal of Nephrology, 42(4), 484–488. https://doi.org/10.1590/2175-8239-JBN-2019-0229
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