Evidence map›Paper›PMID 42832069›Full record

ReviewRheumatology international2026

Nephrotic range proteinuria and rapid progression to end-stage kidney disease in seronegative pauci-immune necrotizing glomerulonephritis masked by cutaneous lesions: a case-based review.

Aleksandra Gałan, Filip Koszałka, Izabela Zakrocka, Amir Nour Mohammadi, Jakub Kleinrok, Agnieszka Korolczuk, Wojciech Załuska

Abstract readCase ReportsReview
In one paragraph

Review in Rheumatology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

7 authors.

Aleksandra GałanStudents' Scientific Club of Nephrology and Transplantology, Medical University of Lublin, Jaczewskiego 8, 20-090, Lublin, Poland.ORCID http://orcid.org/0009-0004-9580-0912
Filip KoszałkaStudents' Scientific Club of Nephrology and Transplantology, Medical University of Lublin, Jaczewskiego 8, 20-090, Lublin, Poland.ORCID http://orcid.org/0009-0007-3487-6464
Izabela ZakrockaDepartment of Nephrology, Medical University of Lublin, Jaczewskiego 8, 20-090, Lublin, Poland. izabela.zakrocka@umlub.pl.ORCID http://orcid.org/0000-0001-5251-7763
Amir Nour MohammadiStudents' Scientific Club of Nephrology and Transplantology, Medical University of Lublin, Jaczewskiego 8, 20-090, Lublin, Poland.ORCID http://orcid.org/0009-0009-2710-513X
Jakub KleinrokDepartment of Clinical Patomorphology, Medical University of Lublin, Jaczewskiego 8b, 20-090, Lublin, Poland.ORCID http://orcid.org/0009-0006-3742-5696
Agnieszka KorolczukDepartment of Clinical Patomorphology, Medical University of Lublin, Jaczewskiego 8b, 20-090, Lublin, Poland.ORCID http://orcid.org/0000-0003-1016-2735
Wojciech ZałuskaDepartment of Nephrology, Medical University of Lublin, Jaczewskiego 8, 20-090, Lublin, Poland.ORCID http://orcid.org/0000-0001-6043-3236

Funding

Uniwersytet Medyczny w Lublinie Uniwersytet Medyczny w Lublinie
6 · The paper itself

Abstract

Antineutrophil cytoplasmic antibodies (ANCA)-negative pauci-immune necrotizing glomerulonephritis (PING) is a rare entity, representing a distinct subset of small-vessel vasculitis. The absence of ANCA does not exclude the diagnosis, and clinical suspicion should remain high in the presence of compatible systemic and renal findings. We present the case of a 22-year-old woman with recurrent, non-specific cutaneous manifestations since early childhood, who was hospitalized for an exacerbation of skin lesions. Laboratory results revealed nephrotic-range proteinuria of 17 g/d [N < 150 mg/d] and a reduced estimated glomerular filtration rate (eGFR) of 47 mL/min/1.73 m² [N > 90 mL/min/1.73 m²]. Renal biopsy results demonstrated cellular crescents, focal segmental tubular necrosis, intense mononuclear inflammatory infiltrates, and segmental proliferation of Bowman's capsule epithelial cells. Direct immunofluorescence yielded negative results for IgG, IgA, IgM, C3, or C1q deposits. Electron microscopy confirmed segmental podocyte foot process effacement and microvillous transformation. Serologic testing was comprehensively negative, specifically confirming the absence of PR3-ANCA, MPO-ANCA, anti-glomerular basement membrane (GBM) antibodies, and serum cryoglobulins. Based on the clinical, histologic, and immunopathologic findings, a definitive diagnosis of isolated ANCA-negative PING was established, although atypical features prompted the consideration of secondary podocytopathy. Methylprednisolone therapy was initiated, but progressive renal deterioration following a substantial loss to follow-up period necessitated renal replacement therapy. This report underscores the diagnostic challenge of ANCA-negative PING, given its absent serologic markers and overlapping features with other glomerular diseases, highlighting the crucial role of renal biopsy in reaching a timely diagnosis.

Indexed as

GlomerulonephritisKidney Failure, ChronicProteinuriaAntibodies, Antineutrophil CytoplasmicBiopsyDisease ProgressionFemaleHumansKidneyNecrosisYoung AdultAntibodies, Antineutrophil CytoplasmicAnti-neutrophil cytoplasmic antibody-associated vasculitisDelayed diagnosisGlomerulonephritis, Pauci-immuneKidney failure, ChronicPurpura

Identifiers

PMID42832069
PMCPMC13638750

What OpenQuestion holds

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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.