ArticleClinical case reports2026
Aortic Valve Perforation in Pediatric Granulomatosis With Polyangiitis: A Case Report.
Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Granulomatosis with polyangiitis, formerly Wegener's granulomatosis, is a rare antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis primarily affecting the respiratory tract and kidneys. Cardiovascular involvement, particularly valvular disease, is rare, especially in pediatric patients. We report a case of a 12-year-old boy newly diagnosed with granulomatosis with polyangiitis, who developed an aortic valve perforation. The patient presented with systemic inflammatory symptoms and was found to have aortic regurgitation secondary to aortic valve perforation. Laboratory findings confirmed markedly elevated c-ANCA titers. Imaging revealed pulmonary involvement, and echocardiography confirmed a perforation in the noncoronary cusp of the aortic valve. Immunosuppressive therapy led to clinical improvement and stabilization of cardiac function, without the need for immediate surgical intervention. This case highlights the importance of considering vasculitis in pediatric patients with systemic inflammation and unexplained cardiac murmurs. Early recognition and prompt immunosuppressive treatment can prevent severe complications.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.