Vena cava anomalies in thoracic surgery

Anomalies of the vena cava represent a rare group of conditions that can occur isolated or in association with other thoracic anomalies, particularly congenital heart diseases (CHD). These conditions are generally asymptomatic and frequently identified as incidental findings during pre-operative computer tomography (CT) or magnetic resonance imaging (MRI). Nevertheless, the knowledge of vena cava anomalies is mandatory for thoracic surgeons and dedicated radiologists to allow safe surgical procedures; if not recognized lethal complications may develop.

We report 3 different cases of vena cava anomalies in patients undergoing lung resection.

Although vena cava anomalies are uncommon, their recognition is mandatory for the radiologists and the surgeons and their unacknowledgment could lead to complications during thoracic surgery intervention. Only rarely anomalies of the vena cava are of clinical concern and these are usually diagnosed accidentally or in association with CHD. However, none of our patients had CHD or other vascular anomalies.

PLSVC is the most common anomaly of the thoracic venous system and occurs approximately in 0.5% of the general population [1]. It is due to the failed regression of the left anterior cardinal vein that generally forms the Marshall’s ligament. In 80–90% of cases PLSVC coexists with a right superior vena cava and in up to 65% of these cases a left innominate vein may be completely absent [2]. In approximately 80–90% of cases, the PLSVC drains into the right atrium through the coronary sinus without hemodynamic consequences. Conversely, when it drains into the left atrium, it may result in right-to-left shunt or in hemodynamic overload on the left atrium with the risk of atrial fibrillation or paradoxical embolization. Although it is the most common thoracic venous anomaly, only few cases of lung cancer resection in patients with a PLSVC have been reported ([3, 4]), generally without complications. However, a large PLSVC may disturb mediastinal lymph node dissection or be misdiagnosed as para-aortic nodal metastasis [5]. There is only one report of a T4 lung cancer that involved a PLSVC, treated by Okur et al. with partial resection of the abnormal vessel [6].

PAPVC is a rare congenital defect characterized by the presence of one or more pulmonary veins that drain in the vena cava. It is due to an incorrect development of the fetal pulmonary vein and it is present in 0.4–0.7% of the population. It is often associated with atrial septal defects [7]. PAPVC is generally located in the right lung and the anomalous vessel usually drains into the SVC, as in our patient. However, anomalous connections with inferior vena cava (IVC), right atrium, azygos vein, portal vein, or hepatic veins have been reported in literature [8]. In particular, Cooper first described in 1836 a Scimitar-shaped vein draining part of the right lung into the IVC [9]. The term “scimitar” refers to the resemblance of the anomalous vein to a Turkish sword on chest X-ray. This anomaly is today known as “Scimitar Syndrome”. Anomalous left-sided PAPVC is less common and in this case the anomalous vessels could drain into the left brachiocephalic vein, coronary sinus, or hemiazygos vein. The surgical indication for PAPVC repair is the presence of left-to-right shunt symptoms or a pulmonary-to-systemic flow ratio (Qp/Qs) greater than 2.0 [10]. However, in patients undergoing lung surgery, this anomaly may require preventive treatment in order to avoid hemodynamic complications and even fatal events. Black et al. described a lethal case of right pneumonectomy with left upper lobe anomalous venous connection [11]. In fact, if the PAPVC is in a different lobe of the planned intervention, a major lung resection could cause heart failure due to increased left-to-right shunt. In these cases, hemodynamic assessment before the intervention could be required to identify those cases requiring preventive PAPVC repair [12]. If the PAPVC is located in the resected lobe, as in our case, no hemodynamic changes should appear. In these patients, lobectomy represents an adequate treatment for both lung cancer and PAPVC [13].

Azygos continuation of the inferior vena cava, commonly called simply “azygos continuation”, is a venous anomaly in which an enlarged azygos vein is the direct continuation of the IVC and drains blood from the caudal districts to the SVC. It affects about 0.1–0.6% of the population, with a slight preponderance in males [14]. It is due to the agenesis of the prerenal IVC. In this situation, the venous return is guaranteed by the supracardinal system that normally forms the azygos system. Both azygos and hemizygos continuation can occur, but azygos continuation is much more common [15]. Often, the azygos vein is dilated as reported in our case. Patients with azygos or hemiazygos continuation usually are asymptomatic and do not required any intervention [16]. However, this anomaly can cause complications during surgical and interventional procedures like right heart catheterization, cardiopulmonary surgery and femoral vein catheter advancement. In thoracic surgery, particular care should be paid in case of esophagectomy. In fact, section of the azygos vein could be required during esophagectomy, and it is usually performed without consequences. Nevertheless, in case of azygos continuation it is mandatory to preserve the integrity of the azygos vein given its role in venous return and its dissection could lead to lethal complications. Martín-Malagón reported a case of hypotension, anuria and death after Ivor Lewis esophagectomy in a patient with unacknowledged azygos continuation [17].

In conclusion, in this case-series we report three different vena cava anomalies whose unacknowledgment produced minor complications in two cases. Even if rare, this represents an important group of anatomical variations that could increase the risk of intra-operatory complications during thoracic surgery, and could lead to lethal consequences. Pre-operative evaluation of the vena cava anatomy at CT scan is mandatory for the surgeon to properly plan the surgery. Furthermore, the identification and isolation of mediastinal great vessels should be performed precociously during any thoracic surgery intervention in order to avoid complications.