Video-assisted thoracoscopic left lower lobectomy in a patient with lung cancer and a right aortic arch
© Wada et al.; licensee BioMed Central Ltd. 2012
Received: 3 June 2012
Accepted: 3 November 2012
Published: 13 November 2012
A right aortic arch is a rare congenital anomaly, with a reported incidence of around 0.1%. A patient with a right aortic arch underwent video-assisted thoracic surgery left lower lobectomy and mediastinal lymph node dissection for squamous cell carcinoma. There was no aortic arch or descending aorta in the left thoracic cavity, but the esophagus. There was no anomaly in the location or branching of the pulmonary vessels, the bronchi, and the lobulation of the lungs. The vagus nerve was found at the level of the left pulmonary artery. The arterial ligament was found between the left subclavian artery and the left pulmonary artery. The recurrent laryngeal nerve was recurrent around the left subclavian artery. A Kommerell diverticulum was found at the origin of the left subclavian artery. The patient experienced no complications. We conclude that video-assisted thoracoscopic lobectomy with mediastinal dissection is feasible for treating lung cancer with a right aortic arch.
A right aortic arch is a relatively rare congenital anomaly, with a reported incidence of around 0.1%. In cases of pulmonary resection for the left lung cancer with a right aortic arch, it is important to locate the vasculature and nerves, especially the recurrent laryngeal nerve (RLN), to avoid injury. We report a case in which we could identify the RLN under video-assisted thoracic surgery (VATS). It was possible to perform lobectomy with mediastinal lymph node dissection without any complications.
A right aortic arch was classified into three types by Stewart et al. Type I, which is a mirror image of the normal anatomical structure, accounts for 59% of cases. This type is often accompanied by visceral inversion. Of type I cases, 98% have congenital heart disease such as tetralogy of Fallot, truncus arteriosus communis, and ventricular septal defect. Type II accounts for 40% of cases, including our case. This type has an aberrant left subclavian artery that originates from the descending aorta. The stem of the left subclavian artery is usually dilated and called a Kommerell diverticulum. Of type II cases, 12% have congenital heart disease. Type III, which involves an isolated left subclavian artery, comprises only about 1% of cases[1, 2].
There have only been seven cases with a right aortic arch, including our case, in which the patient underwent pulmonary resection for left lung cancer. According to the classification of Stewart and colleagues, one of these cases was a type I right aortic arch, and six were type II. Five surgeries were performed through an open thoracotomy and two were performed under VATS. Six patients underwent upper mediastinal lymph node dissection following the lobectomy. In all six cases, the RLN was identified. The RLN was recurrent around the arterial ligament in five cases and around the left subclavian artery in one case. We performed a lobectomy without any difficulty because there was no abnormality in location and branching of the pulmonary arteries, veins, and the bronchi. In the case of left lung cancer, there have been several reports in which mediastinal lymph node dissection was easily performed, compared with right lung cancer, because there was no aortic arch in the left thoracic cavity. However, it was difficult to decide the range of lymphadenectomy and to number the stations of lymph nodes. We interpreted lymph nodes around the arterial ligament as lower paratracheal lymph nodes (#4). Because the lymphatic drainage from the left lung to those areas goes along the tracheobronchus, we thought they should be classified as paratracheal lymph nodes. According to a certain report, lymph nodes around the arterial ligament were interpreted as subaortic lymph nodes (#5) and lymph nodes around the left subclavian artery were regarded as para-aortic lymph nodes (#6).
We believe that this is the first case report in which complete thoracoscopic surgery without a mini-thoracotomy was performed for lung cancer with a right aortic arch. Because we verified the location and branching of the vessels by preoperative three-dimensional computed tomography and understood the anatomy, we could anticipate the site of the RLN. Furthermore, a magnified view by thoracoscopy enabled us to identify the vagus nerve, RLN, and arterial ligament easily and to perform the mediastinal lymph node dissection safely.
Although an advanced technique is required for thoracoscopic surgery, it is feasible to perform VATS lobectomy on patients with a right aortic arch.
Written informed consent was obtained from the patient for publication of this report and any accompying images.
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