Mycobacterium tuberculosis aortic graft infection with recurrent hemoptysis: a case report
© Clerc et al; licensee BioMed Central Ltd. 2008
Received: 04 December 2007
Accepted: 18 July 2008
Published: 18 July 2008
Mycobacterium tuberculosis may cause a large variety of clinical presentations due to its ability to disseminate by contiguity or hematogenously. Tuberculosis may remain undiagnosed for years due to the chronic course of the disease, with potentially life-threatening long-term complications.
In this case report, we describe a tuberculous aortic graft infection in a 72-year-old man documented by polymerase chain reaction and cultures. The patient presented with three episodes of hemoptysis following a remote history of miliary tuberculosis. The infection was treated by graft replacement and prolonged antimycobacterial therapy.
Tuberculous infection of a vascular graft is an uncommon complication, but should be considered in patients with an intravascular device and a history of previous tuberculosis, especially when hematogenous spread may have occurred a few months after surgery, or when an active mycobacterial infection is present in close proximity to the graft.
Mycobacterium tuberculosis is a common pathogen that may cause a large variety of clinical presentations due to its ability to disseminate by contiguity or hematogenously. Tuberculosis may remain undiagnosed for years due to the chronic course of the disease, with potentially life-threatening long-term complications. Here, we report a case of mycobacterial aortic graft infection documented by both polymerase chain reaction (PCR) and culture and we review the literature.
A 72-year-old man with chronic alcohol abuse and hypertension, and who had been a smoker, had had past surgical interventions for atherosclerotic vascular disease (bilateral iliofemoral bypass and abdominal aortic aneurysm repair). In April 2001, the patient presented with severe chest pain due to a descending thoracic aortic aneurysm. At that time, there was no lung abnormality revealed by a computed tomography (CT) scan of the chest. A thoracotomy was performed and a Dacron prosthesis was inserted surgically into the wall of the aneurysm and he had an uncomplicated postoperative course.
Six months later, the patient was hospitalized because of weight loss, night sweats, a dry cough and progressive dyspnea for the past 4 weeks. Chest radiography and CT showed bilateral interstitial lung infiltrates with miliary appearance. No cavitation was documented. A diagnostic bronchoscopy was performed. A Ziehl-Neelsen examination of the lower respiratory tract samples was positive for acid-fast bacilli. PCR and culture of the bronchoalveolar lavage fluid revealed the presence of M. tuberculosis. Hematogenous dissemination of M. tuberculosis was confirmed by a concomitant positive urine culture. Treatment with rifampicin and isoniazid for 6 months, plus pyrazinamide and ethambutol during the first 2 months was given as directly observed therapy, since the strain isolated in culture was susceptible to all major antimycobacterial drugs.
Three weeks later, the patient presented with massive hemoptysis and severe bronchoaspiration requiring intubation and cardiopulmonary resuscitation. Repeated bronchoscopies documented persistent bleeding from the left lower lobe bronchus. Despite the possible occurrence of a fistula between the aorta and the bronchial tree, the treatment was medical since a chest CT scan did not confirm the presence of a fistula. As bleeding resolved spontaneously, hemoptysis was suspected to be only due to lung tuberculosis and not to aortic involvement. Consequently, the patient was not referred for angiography.
Two months later, the patient presented with a recurrence of hemoptysis of about 300 ml while coughing. Bronchoscopy showed blood clots at the orifice of the left lower lobe bronchus. A CT scan confirmed the hypothesis of an aorto-pulmonary fistula by the presence of a hematoma around the distal anastomosis of the aortic graft and contrast enhancement in the anterior wall of the thoracic descending aorta. Despite the absence of active bleeding at the aortography, an endoprosthesis (Talent type 10 cm) was inserted around the level of the distal anastomosis. Five days later, another bronchoscopy did not show any further bleeding. The bronchial tree appeared normal on endobronchial inspection, and no mycobacteria could be grown from the bronchoalveolar lavage. Consequently, the fistula was not attributed to an uncontrolled infection. Antimycobacterial treatment was continued for about 3 months after this second episode of hemoptysis. The patient was then lost to follow-up and the evolution of the periaortic hematoma could not be monitored.
Here we report a PCR and culture-proven case of M. tuberculosis vascular graft infection that presented with recurrent hemoptysis. The infection may have been due to hematogenous spread or to direct extension from contiguous lung infection. The first hypothesis is supported by the occurrence of a miliary tuberculosis 6 months after aortic aneurysm surgery. However, the second hypothesis is more likely given the localization of lung infection near to the aorta and the documented aortopulmonary fistula.
To the best of our knowledge, only four other cases of M. tuberculosis vascular graft infections have been reported to date. The first case was described in 1977 by Wright et al. . Three years after prosthetic aortic graft placement, disruption of the proximal aortic suture and a large pseudo-aneurysm developed. Complete graft excision was required, followed by prolonged antituberculous treatment. Marroni et al.  reported the case of an 80-year-old man with fever of unknown origin that was attributed to endovascular aortic graft M. tuberculosis infection. Interestingly, the evolution was complicated by an aorto-esophageal fistula. Raffetto et al.  described an aortobifemoral Dacron graft infection occurring 2 years after a 6-month course of isoniazid for treatment of latent tuberculosis in an immunocompromised patient who had been treated with high-dose corticosteroids plus infliximab for Takayasu arteritis. A recent report by Sirvanci et al.  describes a case of recurrent false aneurysm of the descending thoracic aorta after surgical treatment by excision and patch repair. Infection of the foreign material was not proven.
Aortic aneurysms are rare complications of tuberculosis. From 1950 to 1995, only 41 cases of aortic mycotic aneurysm caused by M. tuberculosis have been reported . Approximately 75% of cases were consecutive to a contiguous focus of tuberculosis (lymph nodes, lung, vertebrae or paraspinal abscess) whereas 25% of cases were considered to be of hematogenous origin. Several reports have described hemoptysis consecutive to a bronchial communication with a tuberculous aortic aneurysm [6–8]. The accepted treatment of a tuberculous vascular aneurysm is a combination of surgery and antimycobacterial therapy [9–11]. Neither medical nor surgical therapy leads to cure, if used alone . Recently, it was suggested that endovascular treatment for tuberculous infected aneurysm may lead to life-threatening recurrences, because of the absence of tissue debridement . The optimal duration of treatment is unknown because of the lack of controlled trials. Pre-operative antituberculous therapy may decrease the risk of infection of the implanted graft. Interestingly, medical therapy for tuberculosis might not prevent the development of a tuberculous aneurysm .
The case of graft infection reported by Raffetto et al.  was successfully managed by performing debulking surgery followed by long-term antimycobacterial therapy. Thus, graft preservation also seems to be possible with long-term suppressive therapy.
Consequently, we decided to treat the patient for at least 1 year after surgery. Whether the treatment might be stopped at that time will be decided based on clinical evolution, inflammatory parameters (C-reactive protein (CRP), leukocyte count) and radiological imaging. After stopping treatment, we propose to measure CRP and leukocyte count regularly and to repeat a chest CT scan twice a year at least for the next 2 years in order to detect a possible recurrence.
Tuberculous infection of a vascular graft is an uncommon complication, but our case suggests that it should be considered in patients with an intravascular device and a history of previous tuberculosis, especially when hematogenous spread may have occurred a few months after surgery or when an active mycobacterial infection is present in close proximity to the graft.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
polymerase chain reaction.
We thank the patient for supporting the publication of this report. We also acknowledge Dr Philip Tarr for his critical review of this manuscript. GG is supported by the Fondation Leenards through a career award entitled 'Bourse Leenards pour la relève académique en médecine clinique à Lausanne'.
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