Evidence map›Paper›PMID 41165831›Full record

ReviewRheumatology international2025

From ulcerative colitis to amyloid storm: a case-based review.

Sultan Özkurt, Döndü Üsküdar Cansu, Uygar Yildirim, Emel Yaldir, Ahmet Uğur Yalçin, Cengiz Korkmaz

Abstract readCase ReportsReview
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In one paragraph

Review in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sultan ÖzkurtDivision of Nephrology, Department of Internal Medicine, Eskişehir Osmangazi University, Eskişehir, Turkey.ORCID 0000-0001-7552-2186
Döndü Üsküdar CansuDivision of Rheumatology, Department of Internal Medicine, Eskişehir Osmangazi University, Eskişehir, 26480, Turkey. ducansu@hotmail.com.ORCID 0000-0001-6543-3905
Uygar YildirimDivision of Nephrology, Department of Internal Medicine, Eskişehir Osmangazi University, Eskişehir, Turkey.ORCID 0000-0003-0014-4146
Emel YaldirDepartment of Pathology, Eskişehir Osmangazi University, Eskişehir, Turkey.ORCID 0000-0001-7297-9869
Ahmet Uğur YalçinDivision of Nephrology, Department of Internal Medicine, Eskişehir Osmangazi University, Eskişehir, Turkey.ORCID 0000-0003-4357-0823
Cengiz KorkmazDivision of Rheumatology, Department of Internal Medicine, Eskişehir Osmangazi University, Eskişehir, 26480, Turkey.ORCID 0000-0003-2679-0699

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most important complication of familial Mediterranean fever (FMF) are AA amyloidosis and amyloid nephropathy. Amyloid nephropathy typically follows a slow, indolent course. However, "amyloid storm" is a recently described acute condition, characterized by sudden onset of severe proteinuria and rapidly progressive renal failure with markedly acute-phase reactants, progressing over days to weeks into end-stage renal disease (ESRD). Amyloid storm has been rarely reported in the literature. Most cases have occurred in patients with known FMF-related AA amyloid nephropathy. However, it has also been reported as the initial presentation of AA amyloidosis. No standardized treatment guidelines exist, but management has included supportive care, colchicine, and interleukin (IL)-1 blockade. This report presents the first case of amyloid storm associated with ulcerative colitis in the literature. The patient exhibited impaired oral intake and fatigue, alongside acute kidney injury, spot urine proteinuria of approximately 100 g/day, and elevated C-reactive protein levels (CRP 118 mg/L). The diagnosis of AA amyloidosis was made after a kidney biopsy. In addition to starting haemodialysis, the patient was treated with anakinra and colchicine given the clinical presentation indicative of an amyloid storm. Subsequently, the acute-phase reactants decreased and the patient's general health improved, but haemodialysis was still required. After the patient discontinued anakinra treatment, he was re-hospitalized with complaints of fatigue and weakness but died on day 71 after the amyloid storm diagnosis. In our literature review, we identified a total of 36 patients with amyloid storm, 29 of whom were from two separate original studies. According to our review, the frequency of FMF-associated amyloid storm is 5.5%. The majority of patients were male, and while FMF was the most common cause of AA amyloidosis, ankylosing spondylitis, non-FMF autoinflammatory diseases, and ulcerative colitis were among the other causes. Our analysis revealed that infections were the most common triggering factor of an amyloid storm. ESRD rates were found to be up to 67%, and mortality rates ranged from 33 to 67%. This case report aims to highlight the relatively new and little-known concept of amyloid storm, which, despite its rarity, discusses its clinical features, laboratory findings, treatment options, and outcomes based on our case as well as a few cases in the literature.

Indexed as

Acute Kidney InjuryAmyloidosisColitis, UlcerativeFamilial Mediterranean FeverAgedColchicineHumansInterleukin 1 Receptor Antagonist ProteinKidney Failure, ChronicMaleRenal DialysisSerum Amyloid A ProteinColchicineInterleukin 1 Receptor Antagonist ProteinSerum Amyloid A ProteinAmyloidosisFamilial Mediterranean feverInterleukin-1 receptor antagonistsUlcerative colitis

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.