Nefropatia por IgA rapidamente progressiva: um relato de caso / Rapidly progressive IgA nephropathy: a case report

Authors

  • Gabriela Carboni
  • Lucas Brum de Azambuja
  • Cynthia Caetano

DOI:

https://doi.org/10.34119/bjhrv5n2-044

Keywords:

glomerulonefrite por IGA, nefropatia, imunoglobulina A.

Abstract

A Nefropatia por IgA (NIgA) é a glomerulonefrite mais comum no mundo, sendo caracterizada pela produção de imunoglobulina A (IgA) deficiente em galactose e seu depósito na matriz mesangial glomerular. O relato de caso aborda a relevância da pesquisa de glomerulonefrite mesmo em pacientes adulto-jovens com sinais iniciais inespecíficos de edema e hipertensão arterial sistêmica.

References

Fabiano RCG, Pinheiro SVB, Simões e Silva AC. Immunoglobulin A nephropathy: a pathophysiology view. Inflamm Research. 10thed. [S.I.]: Springer International Publishing; 2016.

Rodrigues JC, Haas M, Reich HN. IgA nephropathy. Clinical Journal of the American Society of Nephrology. 4thed. [S.I.: sn]; 2017.

Zhang YM, Zhou XJ, Zhang H. What Genetics Tells Us About the Pathogenesis of IgA Nephropathy: The Role of Immune Factors and Infection. Kidney International Reports. 3thed. [S.I.]: Elsevier Inc.; 2017.

Feehally J. Immunosuppression in IgA Nephropathy: Guideline Medicine Versus Personalized Medicine. Seminars in Nephrology. 5thed. [S.I.]: Elsevier Inc.; 2017.

Yeo SC, Cheung CK, Barratt J. New insights into the pathogenesis of IgA nephropathy. Pediatric Nephrology. 5thed. [S.I.]: Springer International Publishing; 2018.

Trimarchi H, Barratt J, Cattran DC, Cook HT, Coppo R, Haas M, et al. Oxford Classification of IgA nephropathy 2016: an update from the IgA Nephropathy Classification Working Group. Kidney International. 5thed. [S.I.]: Elsevier Inc.; 2017.

Published

03/17/2022

How to Cite

CARBONI, G.; AZAMBUJA, L. B. de; CAETANO, C. Nefropatia por IgA rapidamente progressiva: um relato de caso / Rapidly progressive IgA nephropathy: a case report. Brazilian Journal of Health Review, [S. l.], v. 5, n. 2, p. 4532–4538, 2022. DOI: 10.34119/bjhrv5n2-044. Disponível em: https://ojs.brazilianjournals.com.br/ojs/index.php/BJHR/article/view/45250. Acesso em: 16 oct. 2026.

Issue

Section

Original Papers