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J Thorac Cardiovasc Surg 2009;137:e10-e12
© 2009 The American Association for Thoracic Surgery


Brief Communication

Penetrating ulcer of the aortic arch presenting with hemoptysis

Vassilios S. Avlonitis, PhDa,*, Roger W. Bury, FRCRb, Andrew J. Duncan, FRCSa, Joseph Zacharias, FRCSa

a Department of Cardiothoracic Surgery, Lancashire Cardiac Centre, Blackpool, United Kingdom
b Department of Radiology, Lancashire Cardiac Centre, Blackpool, United Kingdom

Received for publication March 11, 2008; accepted for publication March 23, 2008.

* Address for reprints: Vassilios S. Avlonitis, PhD, Level 9, Plateau Building, Derriford Hospital, Derriford Rd, Plymouth, PL6 8DH, United Kingdom. (Email: avlonitis{at}hotmail.com).

Penetrating aortic ulcers (PAUs) are increasingly recognized as a separate entity. We report a PAU with unusual presentation and discuss difficulties in diagnosis and management.

Clinical Summary

A 58-year-old nonsmoker presented with a 6-month history of hemoptysis and a 1-month history of left-sided chest pain. He was known to have poorly controlled hypertension. Physical examination was unremarkable. Chest radiographic analysis showed a lesion in the left lung apex lying against the aortic arch. Contrast computed tomographic (CT) scanning demonstrated continuity between the lesion and the aortic lumen. Positron emission tomographic analysis confirmed high uptake in the lesion, and the patient was referred to us as having a case of lung cancer with extension into the aorta (Go Figure 1). However, multislice CT analysis with 3-dimensional reconstruction clarified the presence of a PAU in the arch leaking into the lung, with surrounding hematoma (Go Figure 2). The patient continued to experience pain, and we proceeded to surgical intervention.


Figure 1
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Figure 1. Positron emission tomogram demonstrating high uptake in a left upper lobe lung lesion extending into the aortic arch. The lesion was thought to be lung cancer with aortic invasion.

 

Figure 2
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Figure 2. Computed tomographic and 3-dimensional reconstruction showing an aortic ulcer penetrating into the lung.

 
Hypothermic (24°C) cardiopulmonary bypass was established between the right atrium and the right subclavian artery. Myocardial protection was with intermittent antegrade cold blood cardioplegia. The ulcer was full of clot and penetrating into the lung. The clot was sent for culture. The base of the ulcer extended to the descending aorta, adhering to the left lung and the phrenic nerve. Dissection to free the descending aorta was impossible. The aortic wall was thickened, inflamed, and friable. The ulcer was excised, and the aortic defect was patched with Dacron. Because of the poor quality of aortic tissue, the bleeding from the suture line could not be controlled, and therefore the arch was replaced with a Dacron (Golscal, Sulzer Vascutek, UK) graft, leaving an elephant trunk in the descending aorta. An island of aorta containing the innominate and left common carotid arteries was reimplanted onto the arch. The patient was weaned off cardiopulmonary bypass (time, 372 minutes) without inotropes. Because of ongoing coagulopathy, hemostasis was impossible to achieve, despite blood product transfusion. The bleeding only stopped after administration of Factor VIIa.

The patient was extubated within 24 hours and discharged from the intensive care unit. The clot culture grew Staphylococcus aureus. He was started on flucloxacillin for 4 weeks and discharged on day 11. He was readmitted 2 months later with malaise, rigors, fever, and a C-reactive protein level of 80 mg/L. CT scanning showed soft tissue thickening around the graft, resolution of the lung hematoma, and no fluid collection. The results of blood cultures were negative. Based on the previous history, he was started on intravenous flucloxacillin, rifampicin, and gentamicin for 4 weeks. He responded well and was discharged. One year later, he remains well.

Discussion

PAUs result from atheroma, ulcerating and disrupting the internal elastic lamina, burrowing through all aortic layers.1Go They can remain quiescent or lead to dissection, intramural hematoma, aneurysm or pseudoaneurysm formation, fistulation into adjacent organs, or free wall rupture.2Go The most common presentation is with anterior chest pain or intrascapular pain caused by dissection or intramural hematoma.3Go Hemoptysis is an extremely rare manifestation. We could only find one case presenting with hemoptysis in the literature.4Go That case was managed with hypertension control, and the pulmonary hematoma gradually disappeared. In our case, because of persistent pain, we proceeded to surgical intervention. We did not perform a pulmonary resection, expecting the lung hematoma to resolve after aortic repair.

The ulcer penetrating into the lung raises a diagnostic dilemma and can be mistaken for lung cancer invading the aorta. Positron emission tomographic scanning showing activity in the lung suggested the latter. Multislice CT scanning was more accurate in delineating the exact pathology.

At surgical intervention, there was loss of tissue planes between the lung and aortic arch caused by hematoma and inflammation. The thickening of the aortic intima made construction of a hemostatic suture line impossible when patching was attempted. Therefore we excluded the abnormal area with an elephant trunk procedure. Ongoing coagulopathy obliged us to use Factor VII to achieve hemostasis, with impressive results. There are increasing reports of its successful use in cardiac surgery, and we would recommend its use in aortic surgery cases with coagulopathy unresponsive to standard blood product transfusion.5Go

The postoperative course of this patient was uneventful, with the exception of the graft infection. Contamination of the area with lung pathogens was inevitable. In such cases proactive and aggressive management is recommended. Specimens for microbiologic cultures should be obtained intraoperatively, and a prolonged course of antibiotics might be required.

In conclusion, PAUs involving the lung can be mistaken for lung malignancy invading the aorta. Surgical management can be technically challenging, and the possibility of postoperative graft infection must be considered and managed aggressively.

References

  1. Stanson AW, Kazmier FJ, Hollier LH, Edwards WD, Pairolero PC, Sheedy PF, et al. Penetrating atherosclerotic ulcers of the thoracic aorta: natural history and clinicopathologic correlations. Ann Vasc Surg 1986;1:15-23.[Medline]
  2. Troxler M, Mavor AI, Homer-Vanniasinkam S. Penetrating atherosclerotic ulcers of the aorta. Br J Surg 2001;88:1169-1177.[Medline]
  3. Coady MA, Rizzo JA, Hammond GL, Pierce JG, Kopf GS, Elefteriades JA. Penetrating ulcer of the thoracic aorta: What is it? How do we recognize it? How do we manage it?. J Vasc Surg 1998;27:1006-1016.[Medline]
  4. Fukushima M, Seino Y, Yoshikawa M, Ueda Y, Takano T. A case of penetrating aortic atherosclerotic ulcer with hemoptysis. Jpn Heart J 2000;41:781-785.[Medline]
  5. Raivio P, Suojaranta-Ylinen R, Kuitunen AH. Recombinant factor VIIa in the treatment of postoperative hemorrhage after cardiac surgery. Ann Thorac Surg 2005;80:66-71.[Abstract/Free Full Text]




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