Pulmonary artery pseudoaneurysm after a left upper sleeve lobectomy
© Bao et al.; licensee BioMed Central Ltd. 2013
Received: 27 February 2013
Accepted: 27 September 2013
Published: 13 October 2013
A 55-year-old man was re-admitted for persistent hemoptysis and high fever three weeks after an initial left upper sleeve lobectomy for a central squamous lung cancer tumor. Pulmonary artery pseudoaneurysm and pulmonary infection were confirmed by multidetector computed tomography angiography and subsequent emergency completion pneumonectomy. The development of pulmonary artery pseudoaneurysm, secondary to post-operative pulmonary infection and pulmonary vascular manipulation, is rare and prompt surgical manipulation is mandatory.
KeywordsAneurysm Lobectomy Reoperation Trauma
Multidetector computed tomography angiography
Pulmonary artery pseudoaneurysm.
Pulmonary artery pseudoaneurysm (PAP) is a rare but potentially lethal postoperative complication. In total, there have been no more than 50 such cases documented on PubMed, among which, only two cases have evolved after right lung lobectomy [1, 2]. We herein report a case of a PAP following a left upper sleeve lobectomy for a central squamous lung cancer tumor.
A 55-year-old man initially presented to our department with a 6-month refractory dry cough and bloody sputum. Physical examination and past medical history were unremarkable. Chest computed tomography (CT) showed a lesion in the left upper lobe with prominent obstructive lobar pneumonitis. Bronchoscopy revealed a neoplasm on the left superior lobar bronchus and mucosal swelling that extended to the distal end of the left main bronchus. Tissue biopsy confirmed a squamous cell carcinoma and sleeve lobectomy was scheduled after excluding remote metastasis.
A routine sleeve lobectomy was performed via open thoracotomy. Three rings of the distal left lower main bronchus were removed and end-to-end bronchial reconstruction was performed after confirming negative margins by frozen section. The bronchial anastomosis was enveloped tightly with a pedicled parietal pleura. Mediastinal nodal dissection was also completed and included stations 4–9. However, when the anesthesiologist inflated the remnant lung, we noticed an obviously tortuous pulmonary artery due to a lengthy resection of the main bronchus. Therefore, we decided to shorten the artery correspondingly. Considering that a sleeve resection of the pulmonary artery was time-consuming, a latitude-direction enfolding was performed with a continuous running suture with a 5–0 Prolene. Meticulous inspection of the pulmonary artery found neither sub-mucous hematoma nor occlusion or narrowing of the artery. The patient recovered well and was discharged on the ninth post-operative day. The final pathology confirmed squamous cell carcinoma of the left upper lung at stage p-T2N0M0 IB.
Unfortunately, the patient experienced a persistently high fever over 39°C with dark-yellow sputum five days after discharge and mild hemoptysis another two days later. A chest CT examination at a local hospital revealed obvious left pneumonia with moderate pleural effusion. No artery abnormality was reported. Following, imipenem was administered and symptoms of infection resolved one week later; however, the symptom of hemoptysis prolonged and the patient was re-admitted to our hospital.
There was intense adhesion all over the pleural space. Most of the remnant left lower lung was densely consolidated. Dissection of the pulmonary artery trunk was extremely difficult because of the intense adhesion around the aortic window. The pericardium was then opened to free the pulmonary artery trunk; however, the aneurysm ruptured under compression. The left artery trunk had to be closed proximal to the ligamenta arteriosum pulmonalis.
The patient developed postoperative empyema. Pleural lavage with iodine (1:10 diluted, 1,000 mL, twice daily) was administered for 26 continuous days; however, this treatment failed as evidenced by repeated bacteria retention in the pleural effusion. Of note, the empyema eventually healed after 46 days with chest tube water-sealed drainage. No further chemotherapies were administered. Follow-up revealed a normal quality of life and a cancer-free status one year after the first operation for lung cancer.
PAP is an uncommon but life-threatening condition; a variety of causes have been proposed concerning its etiology and most suggest pulmonary pseudoaneurysm is acquired . PAP often occurs after chest trauma, from pulmonary infection, or because of iatrogenic reasons (e.g., interventional treatment) . McQueen et al. proposed that iatrogenic trauma is the most common reason . In the present case, both intrathoracic infection and iatrogenic trauma to the artery were equally contributive.
All cases face life-threatening risks of hemoptysis and suffocation, which makes prompt diagnosis and intervention mandatory to reduce the life threatening risk and save a patient’s life [3–5]. The gold standard for diagnosis of PAP is pulmonary angiography, but this is now largely superseded by non-invasive CT angiography and 3-D reconstruction. In this study, we used MDCTA and 3-D radiography to diagnose the PAP. For early detection of the PAP, we suggest to perform contrast-enhanced CT or pulmonary angiography after sleeve lobectomy.
Hemoptysis is the most frequent and life threatening symptom after pulmonary artery rupture [6, 7]. In the present case, hemoptysis occurred one week after discharge. Fortunately, the intense and extensive pleural adhesions largely limited the expansion and explosion of the pseudoaneurysm into the chest cavity, which would have been otherwise fatal in the early stage of disease development. Treatment of PAP can be surgical through aneurysmectomy and/or lobectomy, or radiological through steel or tungsten coil embolization . In our case, emergency completion pneumonectomy over transcatheter coil embolization management  was selected because of the extensive pulmonary and pleural infection and the grossly consolidated lung. Coil placement may result in luminal obstruction of the left pulmonary artery, and subsequently, lead to lung infarction.
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.
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