ArticleRadiology case reports2026
Right-sided aortic arch with anomalous coronary artery origin and concomitant Stanford type A dissection: A rare case report.
Article in Radiology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- CT-Centered Multimodality Imaging of Arterial Wall Fragility in Acute Aortic Syndromes: A Narrative Review of Imaging Markers and Clinical Implications.Journal of cardiovascular development and disease · 2026Review
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Congenital anomalies of the aortic arch are rare and may be incidentally discovered or present with life-threatening complications. We report a case of a 58-year-old man with hypertension and a remote history of smoking, who presented with sudden, severe chest pain radiating to the back, hypotension, tachycardia, and pallor. Bedside ultrasound revealed moderate pericardial effusion and raised suspicion of aortic dissection. ECG-gated CT angiography (CTA) confirmed a Stanford type A aortic dissection with a right-sided aortic arch (RAA) and anomalous origin of the right coronary artery from the left main coronary artery. Despite supportive management and preparation for emergent surgery, the patient developed progressive shock and died. This case highlights the importance of rapid recognition of rare aortic arch anomalies and concomitant coronary anomalies using advanced imaging, which is critical for surgical planning in acute settings.
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