Evidence map›Paper›PMID 40918843›Full record

ArticleCureus2025

From Dermatology to Nephrology: Unveiling Granulomatosis With Polyangiitis.

Shazia Hussain Miranda, Rafael Davila Pacheco, Elizabeth Zaragoza Ramírez, Kelly Andrea Arenas Sánchez, Delfino Eduardo Ordaz Velázquez

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

5 authors.

Shazia Hussain MirandaInternal Medicine, Centro Medico Nacional 20 de Noviembre, Mexico City, MEX.
Rafael Davila PachecoInternal Medicine, Hospital Regional Lic. Adolfo Lopez Mateos, Mexico City, MEX.
Elizabeth Zaragoza RamírezDermatology, Centro Dermatológico "Dr. Ladislao de la Pascua", Mexico City, MEX.
Kelly Andrea Arenas SánchezInternal Medicine, Centro Medico Nacional 20 de Noviembre, Mexico City, MEX.
Delfino Eduardo Ordaz VelázquezInternal Medicine, Hospital General Dr. Dario Fernandez Fierro, Mexico City, MEX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis, is a rare form of pauci-immune vasculitis that primarily affects the respiratory tract and kidneys, though it can involve virtually any organ system. As a systemic vasculitis, it targets small- and medium-sized blood vessels and is associated with anti-neutrophil cytoplasmic antibodies (ANCA), particularly those directed against proteinase 3 (PR3). Due to its nonspecific symptoms and variable clinical presentation, GPA requires a high index of suspicion for timely diagnosis. Early treatment is essential, as the disease carries a high risk of morbidity and mortality if left untreated. We present a case of a patient with a one-year history of cutaneous lesions who was ultimately diagnosed with GPA, with an unusual concurrent infection by cytomegalovirus (CMV).

Indexed as

cytomegalovirus (cmv)leucocitoclasticnecrotizing vasculitispauci-immune glomerulonephritis (gn)pr3-positive granulomatosis with polyangiitis

Identifiers

PMID40918843
PMCPMC12413906

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.