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J Thorac Cardiovasc Surg 2009;137:e1-e3
© 2009 The American Association for Thoracic Surgery
Brief Communication |
a Cardiology Division, Department of Internal Medicine, Medical University Innsbruck, Innsbruck, Austria
b Department of Cardiac Surgery, Medical University Innsbruck, Innsbruck, Austria
c Institute of Radiology, Medical University Innsbruck, Innsbruck, Austria
Received for publication February 6, 2008; revisions received February 6, 2008; accepted for publication February 17, 2008. * Address for reprints: Thomas Bartel, MD, Cardiology Division, Department of Internal Medicine, University of Innsbruck, Anichstr. 35, A-6020 Innsbruck, Austria. (Email: thomas.bartel{at}i-med.ac.at).
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Coronary sinus (CS) dissection has been described as a complication of pacing electrode implantation only.1
We report here the diagnosis and surgical therapy of spontaneous rupture of a dissected CS in a patient with acute coronary syndrome (ACS) and circumflex artery (CX) to the CS fistula.
ACS was suspected in a 63-year-old man with acute chest pain after physical exertion but with no electrocardiographic signs of acute myocardial infarction. Coronary angiography showed a giant left main coronary artery aneurysm. A very ectatic and calcified CX originated from the aneurysm and drained into a huge CS. There were no coronary stenoses. Transesophageal echocardiographic analysis revealed a possibly hemorrhagic pericardial effusion. Septated echodense structures were found within the CS lumen that were indicative of chronic dissection (
Figure 1, A). Turbulent flow inside the CS was indicative of arterial pressure (Figure 1, B). Cardiac electrocardiographically gated 64-slice computed tomography confirmed a fistula2
passing along the left atrioventricular groove, taking a tortuous course with multiple loops before draining into the CS (Figure 1, C and D). The posterolateral and great cardiac veins were also markedly dilated because of chronic pressure overload (Figure 1, E and F). Consequently, a concealed perforation was thought to have caused hemorrhage. At the time of emergency surgical intervention, approximately 300 mL of hemorrhagic pericardial effusion and blood clots was removed. Manipulation of the multisegmented and enlarged CS was avoided. The fistula was closed, the main stem and CX were dissected, and a large part of the diffuse aneurysm was excised (
Figure 2 and Videos E1, E2 and E3), taking care to leave enough tissue behind next to the orifice of the left anterior descending coronary artery and first diagonal branch, which both originated from the aneurysm back to back. A roof was constructed, with part of the aneurysm wall reinforced by pericardium patches to ensure communication between the left anterior descending coronary artery and the intermediate branch. Subsequently, coronary revascularization was successfully completed, with the left internal thoracic artery bypassing the left anterior descending coronary artery and a saphenous vein graft to the largest obtuse-marginal branch. The patient recovered from surgical intervention uneventfully and was discharged home on postoperative day 6.
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To our knowledge, this case demonstrates for the first time that (1) spontaneous dissection of the CS can occur because of pressure overload as a result of a CX-to-CS fistula and can be adequately visualized by means of transesophageal echocardiography3
; (2) CS dissection can be complicated by pericardial hemorrhage; and (3) CS dissection can mimic not only coronary artery disease by a "steal" phenomenon3
but also ACS caused by painful perforation and should therefore be considered in the differential diagnosis of patients with acute chest pain and pericardial effusion.
Supplementary data
Supplementary data
Supplementary data
Supplementary data
Supplementary data associated with this article can be found in the online version, at doi:10.1016/j.jtcvs.2008.02.036
References
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