- Case report
- Open Access
An uncommon cause of hemoptysis: aortobronchial fistula
Multidisciplinary Respiratory Medicine volume 13, Article number: 25 (2018)
Hemoptysis is a frequent sign of respiratory and non-respiratory diseases. While in most cases the underlying cause is rapidly identified, sometimes the real etiology might be misdiagnosed with dramatic delay in treatment.
A 46-year-old man with hiatal hernia and a history of aortic surgery for aortic coarctation presented with dramatic episodes of hemoptysis and subsequent severe anemia (6,9 g/dl). Digestive and respiratory endoscopy resulted not exhaustive, thus he underwent a contrast-enhanced computed tomography (CT) scan of the chest that showed an aneurysmal dilatation of the descending thoracic aorta with suspected aortobronchial fistula. He underwent cardiac surgery that confirmed the diagnosis and successfully treated the fistula.
We briefly review the literature to raise clinical awareness on this uncommon cause of hemoptysis.
A 46-year-old man with mild esophageal hiatal hernia and a history of cardiothoracic surgery for aortic coarctation presented with several dramatic episodes of hemoptysis with subsequent severe anemia due to aortobronchial fistula, probably a late consequence of the past aortic intervention. He underwent endovascular aortic intervention with successful management of the fistula. Despite being not very frequent as surgical case, aortobronchial fistula is not so rare as seems and unfortunately it is most of the time a fatal complication. Incidence itself can be underestimated, as the majority of cases are not recognized if a postmortem examination is not performed. With this case report we present the diagnostic work up and treatment of this underhand condition in order to better characterize the spectrum of its presentation and to raise clinical awareness on its dramatic consequences.
A 46-year-old man with a recent diagnosis of hiatal hernia was admitted to the Respiratory Diseases Unit of the University Hospital of Modena, Italy for several dramatic episodes of hemoptysis during the previous 30 days, severe anemia (6,9 g/dl) and initial signs of hemodynamic instability (shock index = 1,4). The past medical history revealed that the patient had undergone cardiac surgery for aortic coarctation at the age of 18 without complications neither during the immediate post-operative course nor in the following 20 years follow up period. He was referred to the Respiratory Intensive Care Unit of our Department where blood transfusion was immediately started. A chest X-ray was performed but no significant abnormalities were detected. Thus he underwent urgent digestive endoscopy that revealed a grade B esophagitis according to Los Angeles classification  without any evidence of recent bleeding. Fiber bronchoscopy was then immediately conducted showing limited traces of blood in the bronchial tract afferent to the left upper lobe while no sings of active bleeding was found (Fig. 1). He eventually underwent a contrast-enhanced CT scan of the chest that showed an aneurysmal dilatation of the descending thoracic aorta (Fig. 2) communicating with the left upper bronchus, whose upper posterior hemorrhagic leak determined initial left upper lobe compression and ground-glass opacities with scissural delimitation (Fig. 3). Given the evidence of a communication between aortic aneurism and lung parenchyma or either the tracheobronchial tree the patient was referred to the Cardiac Intensive Care Unit. Thoracic endovascular aortic repair (TEVAR) was preferred rather than a more invasive open surgical approach due to the persistent hemodynamic instability of the patient. Aortobronchial fistula was thus successfully treated with endovascular stent-graft without complications. The patient survived the intervention with uneventful postoperative course and good recovery in less than 30 days. Strict follow up was then started.
Discussion and conclusions
Since its first systematic description, aortobronchial fistula remains a rare condition characterized by acute symptomatology such as hemoptysis sustained by massive endobronchial bleeding [2, 3]. It represents a misdiagnosed disease especially in patients with coexistent clinical complaints with underestimated incidence and more than 30% cases diagnosed at autopsy . In more recent years the etiology of this unusual condition has been better characterized , being now mostly associated with a history of aortic surgery [6, 7]. Studies have showed that complications may occur even many years after the intervention , being lethal sequelae of aortic aneurysmal disease [9, 10]. Fistulas usually involve the left side of the bronchial tree because of the narrow distance between the descending thoracic aorta and the left bronchial hemi system, while on the right side the greater distance between the ascending aorta and bronchial tree make this condition unusual [6, 9]. Nevertheless several case reports describing fistulas from the ascending aorta to the right bronchial tree are reported. Aortic fistulas both into the left and right bronchial tree can follow aortic surgery after unpredictable periods, being often the consequence of pseudo-aneurysms . Once the presence of the fistula has been established a rapid multidisciplinary decision regarding further management should be made considering comorbidity, risk factors and clinical stability. In the past the open surgical approach was the only available with prosthetic graft replacement, patch closure or direct suturing of the aortic side of the fistula . Several complications have been described when patients with aortobronchial fistulas undergo open surgery: stroke, paralysis, respiratory failure, acute renal insufficiency, ischemic cardiac events, acute hemorrhage and secondary graft infection [9, 11]. The reported mortality rates range from 25 to 41% [3, 12]. Thoracic endovascular aortic repair with endovascular stent grafting is a simpler and less invasive approach to exclude the fistulous tract with reduced morbidity and mortality, particularly in high risk and unstable patients . Although less invasive, the technique presents some limitations, mainly due to graft contamination, leakage and migration [11, 13]. Furthermore a variety of combinations of TEVAR with surgical aortic repair have been proposed but further studies are needed to assess the long-term efficacy and safety of these techniques .
This clinical report is intended to raise attention on this uncommon but dramatic cause of massive hemoptysis.
Thoracic Endovascular Aortic Repair
Lundell L, Dent J, Bennett J, Blum AL, Armstrong D, Galmiche JP, et al. Endoscopic assessment of oesophagitis: clinical and functional correlates and further validation of the Los Angeles classification. Gut. 1999;45(2):172–80.
Oppenheimer R, Brotherton L. Aortobronchial fistula: a rare etiology for hemoptysis. Ear Nose Throat J. 2002;81:257–9.
MacIntosh EL, Parrott JCW, Unruh HW. Fistulas between the aorta and tracheobronchial tree. Ann Thorac Surg. 1991;51:515e9.
Dorweiler B, Dueber C, Neufang A, Schmiedt W, Pitton MB, Oelert H. Endovascular treatment of acute bleeding complications in traumatic aortic rupture and aortobronchial fistula. Eur J Cardiothorac Surg. 2001;19:739–45.
Picichè M, De Paulis R, Fabbri A, Chiariello L. Postoperative aortic fistulas into the airways: etiology, pathogenesis, presentation, diagnosis, and management. Ann Thorac Surg. 2003;75:1998–2006.
Ninan M, Hunter S, Parker DJ. Aortobronchial fistula following aortic valve surgery. J R Soc Med. 1994;87:558–9.
Piciche’ M, De Paulis R, Chiariello L. Unusual origin and fistulization of an aortic pseudoaneurysm: “off-pump” surgical repair. Ann Thorac Surg. 1999;68:1406–7.
Kazerooni EA, Williams DM, Abrams GD, Deeb GM, Weg JG. Aortobronchial fistula 13 years following repair of aortic transaction. Chest. 1994;105:1590–4.
Ono M, Takamoto S, Kawauchi M, Egami J, Kotsuka Y. Aortobronchial fistula late after transverse arch replacement. Ann Thorac Surg. 2000;70:964–6.
Razzouk A, Gundry S, Wang N. Pseudoaneurysms of the aorta after cardiac surgery or chest trauma. Am Surg. 1993;59:818–23.
Rassl DM, Suvarna SK, Coopert GJ. Fatal fungal infection complicating aortic dissection after coronary artery bypass grafting. Cardiovasc Surg. 2000;8:79–81.
Leobon B, Roux D, Mugniot A, Rousseau H, Cérene A, Glock Y, et al. Endovascular treatment of thoracic aortic fistulas. Ann Thorac Surg. 2002;74:247.
Kokotsakis J, Misthos P, Athanasiou T, Romana C, Skouteli E, Lioulias A, et al. Endovascular stenting for primary Aortobronchial fistula in association with massive Hemoptysi.S. Tex Heart Inst J. 2007;34(3):369–72.
Chiesa R, Melissano EM, Marone MM, Marrocco-Trischitta MM, Kahlberg A, et al. Aorto-oesophageal and Aortobronchial fistulae following thoracic endovascular aortic repair: a national survey. Eur J Vasc Endovasc Surg. 2010;39:273–9.
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Fontana, M., Tonelli, R., Gozzi, F. et al. An uncommon cause of hemoptysis: aortobronchial fistula. Multidiscip Respir Med 13, 25 (2018). https://doi.org/10.1186/s40248-018-0146-3
- Aortobronchial fistula
- Aortic surgery