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

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 sudden onset 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 intra-vascular 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 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.

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Publication Details

Journal
European Heart Journal - Case Reports
Published
2026-05-12
DOI
https://doi.org/10.1093/ehjcr/ytag338
Primary Topic
Vasculitis and related conditions
Type
article
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article

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

Lauren Shephard, Shanathan Sritharan, Nicolas Zubrzycki, Paul Mansfield et al.
European Heart Journal - Case Reports
Vasculitis and related conditions
article

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

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

Abstract

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 sudden onset 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 intra-vascular 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 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.

European Heart Journal - Case Reports
John Hunter Hospital (AU), Hunter Medical Research Institute (AU), University of Newcastle Australia (AU)
Good health and well-being
Openalex Percentile: Top 5%
Vasculitis and related conditions
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