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J Thorac Cardiovasc Surg 2005;129:951-952
© 2005 The American Association for Thoracic Surgery


Brief Communications

Remodeling operation for unruptured aneurysms of three sinuses of Valsalva

Hidetoshi Akashi, MD*, Eiki Tayama, MD, Keiichiro Tayama, MD, Tomokazu Kosuga, MD, Kazuyoshi Takagi, MD, Shigeaki Aoyagi, MD

Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

Received for publication August 31, 2004; accepted for publication September 7, 2004.

* Address for reprints: Hidetoshi Akashi, MD, the Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 830 Japan (E-mail: akashi{at}med.kurume-u.ac.jp).

Congenital unruptured aneurysms affecting all three sinuses of Valsalva are extremely uncommon.1 Congenital aneurysms of the noncoronary or the right coronary sinus have been described more often in the literature. The distribution of aneurysmal sites has been stated to be approximately 70% for the right coronary sinus, 29% for the noncoronary sinus, and 1% for the left coronary sinus.1 We report here the successful treatment by remodeling procedure of a woman with large, unruptured, isolated aneurysms of the left coronary and noncoronary sinuses of Valsalva and a small aneurysm of the right sinus of Valsalva.

Clinical summary

A symptom-free 62-year-old woman was admitted to the cardiovascular department of our hospital for cardiac examination. An ejection systolic murmur over the left parasternal area was heard, and the chest radiograph delineated an abnormal cardiothoracic ratio. Electrocardiogram showed no ischemic changes and first-degree heart block. Transthoracic echocardiography was performed, and she was found to have two large aneurysms of the left coronary and noncoronary sinuses of Valsalva, with oppression of both atria, trivial aortic and mitral regurgitation, and moderate tricuspid regurgitation. Further, transesophageal echocardiography showed three aneurysms of 60 x 60 mm, 42 x 40 mm, and 16 x 20 mm in size that had extracardiac protrusions from the noncoronary, left coronary, and right coronary sinuses of Valsalva, respectively. Aortography confirmed three saccular aneurysms of the sinuses of Valsalva, and the right and left coronary arteries originating from the aneurysm were also found (Figure 1).


Figure 1
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Figure 1. Preoperative aortography shows largest aneurysm protruding from noncoronary sinus of Valsalva (NA), second largest from left coronary sinus of Valsalva (LA), and smallest from right coronary sinus of Valsalva (RA). LCA, Left coronary artery; RCA, right coronary artery.

 
The aim of surgical management was resection of the three aneurysms of the sinuses of Valsalva and preservation of the aortic valve function. After a longitudinal incision of the pericardium, the aneurysms could not be observed at the cardiac surface but rather were located behind the atrial chambers. Under cardiopulmonary bypass, the aortic root was inspected with particular care, and the aneurysms were circularly incised around the mouth of the aneurysms (left coronary and noncoronary sinuses) from the outside. The communications of the aneurysms and the aortic root were ovoid shaped and 2.5 x 3 cm wide, 2.5 x 3.5 cm wide, and 2.5 x 2 cm wide, corresponding to the left coronary, noncoronary, and right coronary sinuses, respectively. The aortic annulus was not dilated, but all Valsalva walls were aneurysmal, except for the aortic annulus and three commissures. A gel-impregnated Dacron polyester fabric graft (24 mm) was selected, and then the graft was cut into the three crown shapes. After the three commissural points were fixed, a remodeling procedure was performed.

The patient was easily weaned from cardiopulmonary bypass and recovered uneventfully. No aortic regurgitation at all was seen on postoperative aortography (Figure 2).


Figure 2
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Figure 2. Postoperative aortography shows three coronary sinuses of Valsalva after repair. Coaptation of leaflets was intact, and no aortic regurgitation was seen.

 
Discussion

Aneurysms of the left coronary sinus of Valsalva are extremely uncommon and typically protrude and rupture into the pulmonary artery, the left ventricle, or even the epicardium. In this case, the patient had had three aneurysms of the sinuses of Valsalva, including an aneurysm of the left coronary sinus. No similar case involving three congenital unruptured aneurysms of the sinuses of Valsalva has been reported previously.

An unruptured congenital aneurysm of the sinus of Valsalva does not usually cause symptoms, but if it remains untreated it carries some risks, such as right ventricular outflow tract obstruction, coronary artery occlusion, aortic regurgitation, complete heart block, and resistant ventricular tachycardia. We found 22 previously reported cases of extracardiac, isolated, unruptured aneurysms of the left sinus of Valsalva. These were congenital in 12 patients and acquired in 10.2–4 The left sinus alone was affected in 21 patients; there was aneurysmal involvement of all three sinuses in the other patient, but that case was acquired by inflammatory change. Twelve of these 22 patients underwent surgery, and the chosen operative procedure was closure of the mouth of the aneurysm in all cases. This patient was the first to be treated by a remodeling procedure for unruptured congenital aneurysms of all three sinuses of Valsalva. Sarsam and Yacoub5 suggested that remodeling procedure was potentially applicable to aneurysm of the sinus of Valsalva.5 We applied the remodeling procedure because all Valsalva walls were aneurysmal except for the aortic annulus and three commissures, and patch grafting would have been complicated. In addition to these reasons, aortic regurgitation was mild and the aortic annulus had not been dilated.

In conclusion, extracardiac, unruptured Valsalva aneurysms should be surgically repaired, even if asymptomatic, because of the possibility of severe complications. A valve-sparing aortic root remodeling with the Yacoub procedure is potentially applicable to multiple aneurysms of the sinuses of Valsalva, particularly in patients with mild aortic regurgitation or mild or no dilatation of the aortic annulus.

References

  1. Roberts WC. Congenital cardiovascular abnormalities usually "silent" until adulthood. morphologic features of the floppy mitral valve, valvular aortic stenosis, discrete subvalvular aortic stenosis, hypertrophic cardiomyopathy, sinus of Valsalva aneurysm, and the Marfan syndrome. Cardiovasc Clin 1979;10:407-453.[Medline]
  2. Yasuda F, Shimono T, Adachi K, Onoda K, Tani K, Yada I. Surgical repair of extracardiac unruptured acquired Valsalva aneurysms. Ann Thorac Surg 2000;70:1696-1698.[Abstract/Free Full Text]
  3. Antonio L, Enrico P, Gian CP, Flavio S, Davide C, Nario VL. Unruptured aneurysm of the left sinus of Valsalva causing coronary insufficiency. Tex Heart Inst J 2002;29:40-44.[Medline]
  4. Hakami A, Stiller B, Hetzer R. Unruptured congenital aneurysm of the left sinus of Valsalva in a adult with complex left heart malformations. Heart 2003;89:e3.[Abstract/Free Full Text]
  5. Sarsam MA, Yacoub M. Remodeling of the aortic valve anulus. J Thorac Cardiovasc Surg 1993;105:435-438.[Abstract]



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