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Clinical Images

Percutaneous Closure of a Giant Coronary Artery Aneurysm: A Case Summary

April 2026
1557-2501
J INVASIVE CARDIOL 2026;38(4). doi:10.25270/jic/25.00172. Epub October 9, 2025.

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Coronary artery aneurysms (CAAs) are rare anomalies defined as coronary dilations greater than 1.5 times the normal diameter. Giant CAAs are even less common and often pose significant management challenges. We present the successful percutaneous exclusion of a giant right coronary artery (RCA) aneurysm in an older, high-risk patient (Figure 1).

 

Figure 1
Figure 1. Coronary angiography of the patient before the procedure in 2024.

 

An 83-year-old man with hypertension, dyslipidemia, and permanent atrial fibrillation presented with New York Heart Association (NYHA) Class III symptoms. He had a prior RCA aneurysm identified in 2009, along with ectatic coronary vessels and a dual-chamber pacemaker for bradyarrhythmia (Figure 2). The aneurysm may have caused heart failure symptoms because of reduced coronary flow in the RCA. Another possible explanation was that the gigantic aneurysm caused a mild compression of the right atrium and a tricuspid valve regurgitation.

 

Figure 2
Figure 2. Coronary angiography of the patient in 2009.

 

Computed tomography (CT) imaging demonstrated mild compression of the right atrium (Figure 3). Transesophageal echocardiogram (Video 1) confirmed tricuspid regurgitation, which was significantly reduced after closure of the aneurysm (Video 2). No ischemia test was performed, as the aneurysm had shown a considerable increase compared with the previous left heart catheterization, suggesting progressive expansion; therefore, it was considered necessary to proceed with closure without delay.

 

Figure 3
Figure 3. Computed tomography before the procedure showed mild compression of right atrium.

 

Recent imaging showed a significant progression of the RCA aneurysm (2.9 cm), with thrombus and mild compression of the right atrium (Figure 3). Given his surgical risk, a percutaneous approach was selected. Via femoral access, a 7F Amplatz Left 1 guide catheter was used for RCA cannulation. After crossing the lesion with a Sion Blue wire (Asahi) and exchanging for an IRON MAN wire (Abbott) using a microcatheter, a 7F guide-extension catheter facilitated deep vessel engagement and accurate aneurysm mapping (Figure 4). Three PK Papyrus covered stents (Biotronik) were sequentially deployed as follows:

  1. Distal to the aneurysm (4.5 × 26 mm)
  2. Proximal to the aneurysm (5.0 × 26 mm)
  3. Proximal sealing stent to fully exclude the sac (5.0 × 26 mm)

 

Figure 4
Figure 4. IRON MAN wire (Abbott) in the distal right coronary artery.

 

Postdilation with a 5.0 × 12-mm noncompliant balloon ensured full stent apposition (Figures 5-8). Final angiography confirmed complete exclusion of the aneurysm with no contrast leak (Figure 9). At the 1-month follow-up, CT imaging (Figure 10) showed total thrombosis of the aneurysm with no residual flow. The patient reported clinical improvement (NYHA Class I-II) and remained under evaluation for 6 months for tricuspid valve intervention.

This case supports the feasibility and effectiveness of percutaneous aneurysm closure in selected high-risk patients using new generation covered stents. Precise imaging, wire support, and thoughtful technique are key for successful outcomes.

 

Figure 5
Figure 5. Injection through a 7F guide-extension catheter facilitated accurate aneurysm mapping.
Figure 6
Figure 6. Implantation of the first graft stent (4.5 x 26 mm).
Figure 7
Figure 7.  Implantation of the second graft stent (4.5 x 26 mm).
Figure 8
Figure 8. Implantation of the third graft stent (5.0 x 26 mm).
Figure 9
Figure 9. Final angiography confirmed complete exclusion of the aneurysm.
Figure 10
Figure 10. Computed tomography imaging at the 1-month follow-up showed total thrombosis of the aneurysm.

 

 

Affiliations and Disclosures

Konstantinos A. Manousopoulos, MD, PhD1; Panagiotis Varelas, MD1; Petros Dardas, MD2; Nikolaos Mezilis, MD2; Ioannis Tsiafoutis, MD, PhD1

From the 1Hemodynamic Laboratory, General Hospital GHA Korgialeneio Mpenakeio-Hellenic Red Cross, Athens, Greece; 2Hemodynamic Laboratory, St Luke’s Hospital, Thessaloniki, Greece.

Disclosures: The authors report no financial relationships or conflicts of interest regarding the content herein.

Consent statement: The authors confirm that informed consent was obtained from the patient(s) for the intervention(s) described in the manuscript and for the publication thereof, including any and all images.

Address for correspondence: Konstantinos A. Manousopoulos, MD, PhD, Hemodynamic Department, General Hospital GHA Korgialeneio Mpenakeio-Hellenic Red Cross, Athanasaki 2 Street, Athens 11526, Greece. Email: konman7777777@gmail.com