Amyloid Storm: An Uncommon Case of AA Amyloid Nephropathy

Authors

  • Diogo Domingos Nephrology Department, Hospital de Santa Cruz – Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal; Centro Clínico Académico de Lisboa (CCAL), Lisboa, Portugal Author https://orcid.org/0000-0002-7425-5941
  • Ivo Laranjinha Nephrology Department, Hospital de Santa Cruz – Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal; Centro Clínico Académico de Lisboa (CCAL), Lisboa, Portugal; iNOVA4health, NOVA Medical School I Faculdade de Ciências Médicas da Universidade NOVA de Lisboa, Lisboa, Portugal Author
  • Rita Theias Manso Pathology Department, Hospital de Santa Cruz – Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal Author
  • Patrícia Matias Nephrology Department, Hospital de Santa Cruz – Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal; Centro Clínico Académico de Lisboa (CCAL), Lisboa, Portugal; iNOVA4health, NOVA Medical School I Faculdade de Ciências Médicas da Universidade NOVA de Lisboa, Lisboa, Portugal Author
  • Margarida Gonçalves Nephrology Department, Hospital de Santa Cruz – Unidade Local de Saúde de Lisboa Ocidental, Lisboa, Portugal; Centro Clínico Académico de Lisboa (CCAL), Lisboa, Portugal Author

DOI:

https://doi.org/10.71749/pkj.81

Keywords:

Acute Kidney Injury, Amyloidosis, Nephrotic Syndrome, Serum Amyloid A Protein

Abstract

AA amyloidosis is a rare disease caused by tissue accumulation of serum amyloid A (SAA), a protein produced in the liver
in response to chronic inflammation or infection. Kidney manifestations of AA amyloidosis usually develop gradually.
The authors report a case of a 77­‑year­‑old patient with a previous diagnosis of multifactorial chronic kidney disease and
bronchiectasis, who developed sudden onset nephrotic syndrome and KDIGO stage 3 acute kidney injury shortly after
the diagnosis of acute pyelonephritis. A kidney biopsy confirmed the diagnosis of renal AA amyloidosis. Progressive
kidney dysfunction ensued, with the need to begin kidney replacement therapy eleven months after the initial diagnosis.
This type of renal AA amyloidosis (referred to as “amyloid storm”) has been reported in patients with familial Mediterra‑
nean fever but was not previously described in AA amyloidosis of other etiologies. The prognosis is poor, especially after
dialysis initiation, and more studies are needed to develop strategies to delay its progression and improve outcomes.

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References

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Published

29-04-2025

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Section

Case Report

How to Cite

Amyloid Storm: An Uncommon Case of AA Amyloid Nephropathy. (2025). Portuguese Kidney Journal. https://doi.org/10.71749/pkj.81

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