Evidence map›Paper›PMID 42253887›Full record

ArticleEuropean heart journal. Case reports2026

Intracoronary imaging demonstrating vasculitis as a rare cause of myocardial infarction: a case report.

Lauren Shephard, Shanathan Sritharan, Nicolas Zubrzycki, Paul Mansfield, Nicholas Collins, Nicholas Whitehead, Andrew J Boyle, Mohammed Al-Omary

Abstract readCase Reports
In one paragraph

Article in European heart journal. 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.

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

8 authors.

Lauren ShephardCollege of Health, Medicine and Wellbeing, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.ORCID https://orcid.org/0000-0002-4450-7052
Shanathan SritharanCollege of Health, Medicine and Wellbeing, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Nicolas ZubrzyckiDepartment of Cardiovascular Medicine, John Hunter Hospital, Lookout Road, New Lambton Heights, NSW 2305, Australia.
Paul MansfieldCollege of Health, Medicine and Wellbeing, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Nicholas CollinsCollege of Health, Medicine and Wellbeing, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Nicholas WhiteheadCollege of Health, Medicine and Wellbeing, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Andrew J BoyleCollege of Health, Medicine and Wellbeing, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.
Mohammed Al-OmaryCollege of Health, Medicine and Wellbeing, The University of Newcastle, University Drive, Callaghan, NSW 2308, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Proteinase 3 (PR3)-positive anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, most associated with granulomatosis with polyangiitis (GPA-'Wegener's), is a rare, systemic autoimmune disorder. In this report, we describe an uncommon case of thrombus formation in ANCA vasculitis. Case summary: A 20-year-old male with well-controlled type 1 diabetes presented with the sudden onset of chest pain. The patient had a recent diagnosis of ANCA-associated vasculitis with multisystemic involvement and had completed induction rituximab therapy and pulse of methylprednisolone, before starting moderate dose oral prednisolone and avacopan in the week prior. Electrocardiogram demonstrated inferolateral ST-elevation myocardial infarction; an initial computed tomography aortogram excluded aortic dissection and illustrated mural thickening and luminal irregularity involving the left anterior descending artery. Coronary angiography confirmed distal left circumflex artery occlusion. Given age, stenosis location, vessel size and underlying vasculitis diagnosis, the lesion was prepared with semi-compliant balloon dilatation and then treated with drug-coated balloon angioplasty. Follow-up imaging 4-days later revealed residual left circumflex coronary artery thrombus and vessel wall inflammation, along with inflammation in the left anterior descending artery. Additional intravascular imaging at 6-months showed ongoing intimal thickening. Discussion: PR3-positive disease presenting as a myocardial infarction is an exceedingly rare cardiac manifestation of small vessel vasculitis. This case highlights the role of intracoronary imaging in assessing ANCA-associated vasculitis, which has not, to our knowledge, been previously detailed in the literature. Importantly, this case underscores the importance of characterising the underlying pathology to treat reversible causes and demonstrates the novel use of using drug coated balloons in such cases.

Indexed as

ANCA-associated vasculitisCase reportCoronary vasculitisIntracoronary imagingMyocardial infarction

Identifiers

PMID42253887
PMCPMC13237557

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