Evidence map›Paper›PMID 42329457›Full record

ReviewRheumatology international2026

Granulomatosis with polyangiitis presenting with rare urogenital involvement: a case based review.

Natalia Muklewicz, Ilona Tadulewicz, Iwona Aponowicz, Katarzyna Sienkiewicz, Michał Kujach, Michał Chmielewski, Anna Masiak

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.

Natalia Muklewicz *University Clinical Centre, Gdansk, Poland.ORCID http://orcid.org/0009-0002-4644-7935
Ilona Tadulewicz *University Clinical Centre, Gdansk, Poland.ORCID http://orcid.org/0009-0000-7742-5320
Iwona AponowiczDepartment of Rheumatology, Specialist Hospital in Koscierzyna, Koscierzyna, Poland.
Katarzyna Sienkiewicz2nd Division of Radiology, Faculty of Health Sciences with the Institute of Maritime and Tropical Medicine, Medical University of Gdańsk, Gdansk , Poland.ORCID http://orcid.org/0009-0009-6301-4497
Michał KujachDepartment of Pathomorphology, Specialist Hospital in Koscierzyna, Koscierzyna, Poland.
Michał ChmielewskiDepartment of Rheumatology, Clinical Immunology, Geriatrics and Internal Medicine, University Clinical Centre, Medical University of Gdańsk, Gdansk, Poland.ORCID http://orcid.org/0000-0001-8126-8786
Anna MasiakDepartment of Rheumatology, Clinical Immunology, Geriatrics and Internal Medicine, University Clinical Centre, Medical University of Gdańsk, Gdansk, Poland. anna.masiak@gumed.edu.pl.ORCID http://orcid.org/0000-0001-6687-2408

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Granulomatosis with polyangiitis (GPA) is a rare systemic necrotizing vasculitis, typically involving the upper and lower respiratory tract and kidneys. Urogenital manifestations are uncommon (< 2%) and frequently mimic malignancy. We describe a female patient in whom GPA initially presented with urogenital manifestations and review the available literature regarding urogenital involvement in the course of GPA. We describe the case of a 58-year-old woman with granulomatosis with polyangiitis initially presenting as a bladder mass, leading to radical cystectomy before the autoimmune etiology was recognized. Over time, the disease evolved to include typical manifestations. Despite multiple relapses under conventional immunosuppression therapy, sustained remission was achieved with rituximab. A literature search of PubMed, Scopus, Embase and Directory of Open Access Journals was performed using predefined keywords related to GPA and urogenital involvement. Exclusion criteria included article language other than English, male patients and kidney involvement. Data were extracted on clinical presentation, diagnostic approach, treatment, and outcomes. We identified 40 female patients with GPA involving the urogenital tract, including our case. The cervix (45%), bladder, and urethra were the most commonly affected sites. In 48 of cases, urogenital involvement was the first manifestation of GPA, frequently mimicking gynecologic or urologic malignancy. Unnecessary surgical interventions were reported in 43% of patients. Corticosteroids and cyclophosphamide were the most commonly used therapies, while rituximab was effective in refractory disease. Urogenital involvement in GPA is rare, often misdiagnosed as malignancy, and associated with significant diagnostic and therapeutic challenges. Heightened awareness of this atypical presentation and early rheumatologic evaluation is crucial to prevent unnecessary invasive procedures. Rituximab represents an effective treatment option in relapsing or refractory cases.

Indexed as

Granulomatosis with PolyangiitisCystectomyFemaleHumansImmunosuppressive AgentsMiddle AgedRituximabTreatment OutcomeImmunosuppressive AgentsRituximabBladder massGranulomatosis with polyangiitisRituximabUrogenital involvement

Identifiers

PMID42329457
PMCPMC13287143

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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.