Brazilian Journal of Nephrology (Aug 2020)

Idiopathic nodular glomerulosclerosis and differential diagnosis

  • Sergio Raúl Alvizures Solares,
  • Héctor Raúl Ibarra-Sifuentes,
  • María Guadalupe Ramírez Ramírez,
  • Giovanna Yazmin Arteaga Muller,
  • Jesús Cruz Valdez

DOI
https://doi.org/10.1590/2175-8239-jbn-2019-0229
Journal volume & issue
Vol. 42, no. 4
pp. 484 – 488

Abstract

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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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