Amyloid Storm: An Uncommon Case of AA Amyloid Nephropathy

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.

Institutions

Publication Details

Journal
Portuguese Kidney Journal (PKJ)
Published
2025-02-22
DOI
https://doi.org/10.71749/pkj.81
Citations
1
Primary Topic
Amyloidosis: Diagnosis, Treatment, Outcomes
Type
article
Field-Weighted Citation Impact
0.81
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Amyloid Storm: An Uncommon Case of AA Amyloid Nephropathy

1 citations
Portuguese Kidney Journal (PKJ)
Amyloidosis: Diagnosis, Treatment, Outcomes
0.81
article

Amyloid Storm: An Uncommon Case of AA Amyloid Nephropathy

article en
1 citations

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.

Portuguese Kidney Journal (PKJ)
Hospital de Santa Cruz (PT), Centro Hospitalar de Lisboa Ocidental (PT), Universidade Nova de Lisboa (PT)
No poverty
Openalex Percentile: Top 21%
Amyloidosis: Diagnosis, Treatment, Outcomes
0.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Amyloid Storm: An Uncommon Case of AA Amyloid Nephropathy · Portuguese Kidney Journal (PKJ) (2025) | TGRS Research Map | TGRS