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J Thorac Cardiovasc Surg 2007;133:1643-1644
© 2007 The American Association for Thoracic Surgery
Brief Communication |
a Department of Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, The Netherlands
b Department of Radiology, St Antonius Hospital, Nieuwegein, The Netherlands.
Received for publication November 10, 2006; revisions received November 29, 2006; accepted for publication December 7, 2006. * Address for reprints: B. P. van Putte, MD, PhD, Department of Cardiothoracic Surgery, St Antonius Hospital, Koekoekslaan 1, Nieuwegein, The Netherlands. (Email: bvanputte{at}yahoo.com).
A 59-year-old man was admitted to our hospital with a history of coronary artery bypass grafting 2 years before. On admission, he reported having exercise-induced dyspnea (New York Heart Association class III). Physical examination revealed decreased breath sounds at the left lower pulmonary fields and blood analysis showed a hemoglobin level of 7.7 mg/dL. Contrast-enhanced computed tomography (CT) (Figure 1, B) and magnetic resonance imaging (MRI) (Figure 1, A) of the aorta showed an aneurysm of 9.7 x 8.0 cm located on the left lateral aspect of the lower descending aorta. The presence of fluid in the left pleural space was suggestive of a leaking aortic aneurysm. Therefore, the patient was urgently treated with two aortic endoprostheses (Valiant 30 x 30 and 38 x 38 mm; Medtronic, Inc, Minneapolis, Minn) successfully inserted under radiographic control.
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The postoperative course was complicated by a necrotic gall bladder, which required a cholecystectomy. The patient did not receive adjuvant radiotherapy because the large size of the radiation field would have resulted in a disproportional risk of cardiotoxicity and no response was expected from chemotherapy. After 6 months, the patient was in good condition and follow-up CT did not show evidence of recurrent disease (Figure 3).
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The diagnosis of aortic sarcoma is rare and is established only during or after operation or at autopsy.1
Most aortic sarcomas originate from the intimal layer and are characterized by an intraluminal growth pattern often resulting in partial aortic occlusion and embolization.
In this case, the initial CT was characterized by an intramural process originating from the lateral side of the descending aorta in combination with a large amount of pleural fluid present at the same side. Together with findings from history and physical examination, this presentation of an aortic sarcoma mimicked a symptomatic and leaking aortic aneurysm. Owing to the extremely low incidence of an aortic tumor, however, the diagnosis of a symptomatic aneurysm was made at initial presentation and the final diagnosis of aortic sarcoma was therefore delayed for 3 months.
During the second admission, retrospective comparison of the CT and MRI revealed an increased size of the aortic mass but no signs of endoleakage (Figure 1). Furthermore, the aortic mass was characterized by a distinct heterogeneous appearance present on the lateral side of the aorta. Furthermore, the mass was draped lobulated around the lumen of the aorta. These findings were suggestive of a tumor. The diagnosis of a tumor was strengthened by demonstration of vascularity in the mass by Doppler ultrasonography and enhancement of the mass on MRI. The malignant nature of the tumor was highly suspected as a result of the high uptake on PET scan; to our knowledge, a preoperative PET scan of an aortic sarcoma has never been described. Owing to the low incidence of aortic sarcoma, the premortem diagnosis and imaging of aortic sarcoma is highly unusual.
Although aortic sarcoma remains an exceptional disease, its presence should be considered in a case of atypical presentation of a symptomatic aortic aneurysm. Furthermore, a high degree of uncertainty is needed when interpreting imaging techniques in these patients.2
References
This article has been cited by other articles:
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C. Rusthoven, M. L. Shames, M. M. Bui, and R. J. Gonzalez High-Grade Undifferentiated Pleomorphic Sarcoma of the Aortic Arch: A Case of Endovascular Therapy for Embolic Prophylaxis and Review of the Literature Vascular and Endovascular Surgery, July 1, 2010; 44(5): 385 - 391. [Abstract] [PDF] |
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