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J Thorac Cardiovasc Surg 2003;126:883-885
© 2003 The American Association for Thoracic Surgery


Brief communications

Successful treatment of a mycotic aortic arch aneurysm associated with an isolated left vertebral artery

Yuji Naito, MDa,*, Masato Nakajima, MDa, Hidenori Inoue, MDa, Eiki Mizutani, MDa, Koji Tsuchiya, MDa

a Department of Cardiovascular Surgery, Yamanashi Central Hospital, Kofu-shi, Japan

Received for publication January 20, 2003; accepted for publication March 17, 2003.

* Address for reprints: Yuji Naito, MD, Department of Cardiovascular Surgery, Yamanashi Central Hospital, 1-1-1, Fujimi, Kofu-shi, Yamanashi, Japan, 400-0027
ujinaito{at}aol.com

Mycotic aneurysms are rare in this age of antibiotics, but they are life-threatening. The isolated left vertebral artery (ILVA) is a left vertebral artery originating directly from the aortic arch. It is one of the most common aortic arch branch anomalies, occurring in about 4% of the general population. The case report presented here is of a mycotic aortic arch aneurysm associated with an ILVA.

Clinical summary

A 65-year-old man was admitted to another hospital for investigation into back pain that had lasted for a few hours and disappeared spontaneously. He had reported a cough and febrile illness about 2 months earlier. He was not receiving any drugs, and his medical history was unremarkable. Chest computed tomographic findings led to a diagnosis of aortic arch aneurysm, and the patient was referred to us for surgical treatment. The patient was afebrile on admission. Vital signs were normal, as were cardiopulmonary sounds. Cardiovascular examination revealed a good pulse without bruits at all sites. Laboratory tests showed a leukocyte count of 9500 x 109 cells/L and a C-reactive protein level of 7.62 mg/dL. Chest radiography revealed a mildly enlarged mediastinal shadow and normal cardiothoracic ratio. Chest computed tomographic scan (Figure 1, A and B) confirmed a multisaccular aneurysm of the aortic arch, and both magnetic resonance angiography (Figure 2) and digital subtraction angiography (Figure 1, B) depicted an ILVA arising from the aneurysmal wall.



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Figure 1. Preoperative computed tomography (A, B) revealed multisaccular aneurysm of aortic arch suggestive of mycotic aneurysm. Digital subtraction angiography (C) revealed ILVA (arrow) arising from aneurysmal wall.

 


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Figure 2. A, Preoperative magnetic resonance angiography showed ILVA (arrow) arising from aneurysmal wall. B, Postoperative magnetic resonance angiography showed reconstructed ILVA (arrow) to be patent.

 
We performed semiurgent surgery because the patient was at risk for rupture of the aneurysm. During surgery, dense adhesion around the aortic arch vessels was noted, probably caused by infection-induced inflammation. Total arch replacement with a 4-branched collagen-pretreated aortic arch graft (Hemashield Branched Graft; Meadox Medical, Oakland, NJ) was completed with selective cerebral perfusion. Cardiopulmonary bypass was established with ascending aortic and single right atrial cannulation. Under a condition of circulatory arrest at a rectal temperature of 28°C, the aneurysm was opened, then selective cerebral perfusion was started through the innominate and left common carotid arteries. The aneurysmal wall was thickened and edematous, with some atherosclerotic lesions containing druses. The left subclavian artery (LSA) and ILVA were simply clamped. After careful inspection of the aorta, dissection was extended for utmost eradication of infected tissue toward healthy-looking aorta, where distal anastomosis was completed. After proximal graft anastomosis and LSA repair were completed, the shortened ILVA was reconstructed with a saphenous vein graft interposed between the native ILVA and the side of the graft branch anastomosed to the LSA. After all cervical vessels were reconstructed, cardiopulmonary bypass was stopped. The cardiopulmonary bypass, selective cerebral perfusion, circulatory arrest, and aortic crossclamping times were 164, 97, 49, and 82 minutes, respectively. Streptococcus pneumoniae, susceptible to cefazolin and to meropenem, was cultured from aortic lesion tissue. The patient was treated intravenously with 1 g cefazolin during surgery and 2 g meropenem after surgery. After 2 weeks of antibiotic therapy, he was discharged on postoperative day 19. His 6-month follow-up examination showed no recurrence of the infection.

Discussion

Mycotic aortic aneurysm is an extremely rare complication of arterial infection, accounting for fewer than 1% of aortic aneurysm repairs. The bacterial organisms commonly identified include Staphylococcus aureus, Staphylococcus epidermidis, Salmonella species, Streptococcus species, Haemophilus influenzae, Pseudomonas species, Candida species, and Escherichia coli.1 Isolation of S pneumoniae in the mycotic aneurysm seems to be rare; we have found only a few reports associated with this pathogen.2,3

It has been suggested that in situ insertion of cryopreserved aortic homograft would reduce the postoperative infection rate and improve survival of this group of high-risk patients4; however, most patients with mycotic aneurysm require emergency intervention, and access to a tissue bank is not feasible. In certain circumstances, such as active purulent infection by S pneumoniae, homografts have been reported to fail.3

How to deal with the ILVA is debated. We decided to preserve our patient's ILVA for two reasons. One was that in certain aortic arch anomalies the left common carotid artery does not supply normal blood flow, and the ILVA compensates for this.5 Another was that if the vertebrobasilar axis is a dominant left axis or if communication at the arterial circle of Willis is poor because of another arterial lesion, elimination of the ILVA can cause ischemia of the brainstem and cerebellum. The approaches to ILVA reconstruction include en bloc reconstruction of the arch branches, direct anastomosis to the graft branch corresponding to the LSA, and direct anastomosis to the native LSA.6,7 Although there are no published long-term results concerning the patency of the reconstructed ILVA, we used a saphenous vein graft interposed between the ILVA and graft branch.

References

  1. Svensson LG, Crawford ES. Cardiovascular and vascular disease of the aorta. Philadelphia: Saunders; 1996.
  2. Nijs A, Vandekerkhof J, Cartuyvels R, Magerman K, Mewis A, Peeters V, et al. Streptococcus pneumoniae–infected aneurysm extending from a persistent lobar pneumonia: case report and review of the literature. Eur J Clin Microbiol Infect Dis. 2002;21:389–392[Medline]
  3. Berdat PA, Malinverni R, Kipfer B, Carrel TP. Homograft failure in mycotic aortic aneurysm caused by Streptococcus pneumoniae. Ann Thorac Surg. 1998;66:1818–1819[Abstract/Free Full Text]
  4. Vogt PR, Brunner-La Rocca HP, Carrel T, von Segesser LK, Ruef C, Debatin J, et al. Cryopreserved arterial allografts in the treatment of major vascular infection: a comparison with conventional surgical techniques. J Thorac Cardiovasc Surg. 1998;116:965–972[Abstract/Free Full Text]
  5. Ad N, Lee P, Cox JL. Type A aortic dissection with associated anomaly of the carotid and vertebral vessels. J Thorac Cardiovasc Surg. 2002;123:570–571[Free Full Text]
  6. Kazui T, Washiyama N, Muhammad BA, Terada H, Yamashita K, Takinami M. Improved results of atherosclerotic arch aneurysm operations with a refined technique. J Thorac Cardiovasc Surg. 2001;121:491–499[Abstract/Free Full Text]
  7. Nonami Y, Tomosawa N, Nishida K, Nawata S. Dissecting aortic aneurysm involving an anomalous right subclavian artery and isolated left vertebral artery: case report and review of the literature. J Cardiovasc Surg (Torino). 1998;39:743–746[Medline]



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