The mediastinum is a complex region inside the thorax that contains a wide variety of organs and, consequently, may be affected by a great number of disorders. Mediastinum is classically divided into specific compartments. This arbitrary division aids in the definition of differential diagnoses at the initial presentation and facilitates the treatment plans (1). The classical anatomical classification of the mediastinum reports four compartments: anterior, superior, middle and posterior. However, the anterior and the superior compartments are often described as a single anatomical region due to numerous disorders that may affect both concomitantly. The anterior-superior mediastinum is a site for a wide variety of tumors, which arise from its main cellular components, deriving from the thymus, lymph nodes and, rarely, ectopic tissues and embryonic remnants (2). As reported by Takeda et al., the most common location of neoplasia in the mediastinum is the antero-superior compartment that accounts for 68% of the mediastinal tumors in adults, whereas the posterior mediastinum is more frequently affected in children (3). Tumors of pediatric and adult age show different demographical, clinical and histological spectrum. In infants and children, the primary mediastinal masses in order of decreasing frequency are neurogenic tumors, germ cell tumors (GCTs) and pleuro-pericardial or enterogenous cysts (4). The most common primary tumor of the antero-superior mediastinum, in adults, are thymomas that accounts for more than 50% of the mediastinal masses followed by lymphoma, GCT and parathyroid adenoma that rarely required an extended surgery. Nevertheless, the antero-superior mediastinum is, often, involved large metastatic lymph nodes especially in advanced lung and thyroid cancer. Since mediastinal tumors, especially bulky masses, are very uncommon, accounting for less than 5% of all the tumors, scarce literature is available regarding this matter. Antero-superior large mediastinal tumors offer both diagnostic and therapeutic challenges, due to the complex anatomy of the mediastinum, especially in case of compression or infiltration of vital surrounding structures (5). Since mediastinal space is narrow, up to 60% of all tumors involving the anterior mediastinum are symptomatic at presentation as consequence of the mechanical compression or infiltration of the neighboring organs (6) as reported in Table 1. In addition, the management of some patients might be further complicated by the mediastinal mass syndrome (MMS) that represents a life-threating condition characterized by acute respiratory and hemodynamic failure, due to obstruction of airways and the compression of the heart or major vessels. This syndrome is a life-threating condition that may became even more dramatic by induction of anesthesia or positional changes during surgery (7). Therefore, a thorough pre-operative study is essential to assess the anatomy and exact relationship of the tumor with the surrounding mediastinal structures and to plan, in detail, the eventual operation. Not to forget clinics and/or exams to exclude potential paraneoplastic syndromes associated to the mediastinal masses.
The anatomical assessment of the mediastinum is conducted in most cases by the computed tomography (CT) scan of the chest. This examination allows a detailed definition of the tumor’s features, from its location to relations with the adjacent structures; moreover, the use of the intravenous contrast highlights the vascularization (8). When needed, further examinations are required to define the relation of the tumors with other structures. The magnetic resonance imaging (MRI) is more useful in soft tissue differentiation and in estimation of the chest wall invasion, while transthoracic echocardiography (TTE), transesophageal echocardiography (TEE) and the more recent electrocardiography (ECG)-gated cardiac CT and MRI improve the assessment of the compression or the involvement of the heart or the main vessels by reducing the cardiac motion artifacts (9,10). Fluorodeoxyglucose positron emission tomography (FDG-PET) has a fundamental role in the diagnostic evaluation of mediastinal tumors, with impact on diagnosis, staging and prognosis but plays a marginal role regarding the anatomical assessment of the mediastinum (11); while tracheo-bronchial tree could be thoroughly evaluated by the bronchoscopy that could be performed also during surgery (12). Large mediastinal tumors are often highly vascularized with a significant risk of bleeding or technical complication during surgery. The blood supply is extremely variable, possibly derived from branches of the internal mammary artery, bronchial arteries, thyrocervical trunk, intercostal vessels, phrenic nerve vessels, pulmonary artery, and even from coronary arteries (13-15). MRI or CT scan with intravenous contrast may provide detailed information about the tumor’s vascularization and, in case of invasion of the superior vena cava (SVC), on the collateral circulation (16). Recently, some authors advocated the imaging-guided embolization of the tumor’s vessels as a useful pre-operative treatment in order to reduce the operative blood loss and, sometimes, the tumor mass, although no large studies are available on this matter (17,18). Preoperative biopsy should be avoided when the anterior mediastinal tumor has well-demarcated borders and could easily be resected completely because the increased possibility of tumor seeding. On the other hand, this approach cannot be used in extended large masses presenting as inoperable cases; where neoadjuvant therapy may improve the resectability or facilitate the surgical resection by “setting free” the surrounding structures involved. Both thymomas and primary mediastinal non-seminomatous GCTs are chemo- and radio-sensitive. When presented as extended mediastinal masses, multimodality treatment may be the approach of choice, consisting of neoadjuvant chemo- or radiation therapy followed by surgical resection of residual disease, furthermore, most of lymphoproliferative malignancies are completely treated by systemic chemotherapy. The role and the effectiveness of preoperative treatment is strictly related to the histopathological diagnosis obtained through a fine-needle aspiration (FNA) and core needle biopsy, or by more invasive surgical procedures for biopsy, including anterior mediastinotomy, mediastinoscopy, and video-thoracoscopy. Additional tests such as laboratory studies, the most common of which include α-fetoprotein (α-FP), β-human chorionic gonadotropin (β-HCG), and lactate dehydrogenase (LDH) for the non-seminomatous GCTs and antibodies anti-acetylcholine receptor and anti-muscle-specific tyrosine kinase for the thymoma related to syndrome myasthenia gravis can play an important role. An excellent work-up scheme has been described by Li et al. in 2016 (5) and reported with some changes in Figure 1.
In case of large mediastinal masses, a good exposure is mandatory to achieve a total control of all structures that may be involved and avoid major complication. Sternotomy is the optimal approach to anterior mediastinal tumors, even in the presence of pulmonary involvement. Any operation on both lung parenchyma, on the main airway or all the great vessels, pericardium could be performed through this approach. Moreover, sternotomy is essential whenever extracorporeal circulation (ECC) is required. This midline approach can be extended to a thoracotomy (hemi-clamshell incision) or may be combined with a cervicotomy where necessary (Figure 2). Rarely have been described other approaches as the thoracotomy or the clamshell incision, while a minimally invasive technique should be considered only with a diagnostic purpose rather than for a radical surgery especially for tumors larger than 10 cm (5,19). The main goal of extended surgery of antero-superior mediastinum is be as radical as possible. Absolute contraindications to resection of mediastinal masses are invasion of the myocardium, while the involvement of great vessels or long tracheal segment should be evaluated case-by-case. Any infiltrated structure should be resected and reconstructed when possible. Lung parenchyma could be resected easily, ranging from a wedge resection using a stapler to a lobectomy until a pneumonectomy (eventually, requiring an intrapericardially suture when the hilum is invaded), along with the mediastinal pleura and pericardium. In large pericardial resections a prosthetic mesh should always be placed to avoid the potential migration of the heart through the defect into the thoracic cavities, especially after a pneumonectomy. Phrenic nerve is usually sacrificed when infiltrated, even if it must always be preserved on at least one side, especially if pulmonary resection is planned, but some authors reported an effective technique in sparing the nerve by a gentle peeling of the perineural layers to avoid further respiratory complication, especially in patient with an impaired pulmonary function or myasthenia gravis (20). Of the great vessels, the SVC and the brachiocephalic veins are the most commonly affected, although with varying degrees of involvement, ranging from partial compression or invasion, to the development of SVC syndrome (SVCS) when the vein is completely occluded by the tumor. In general, most authors advocated a total SVC replacement with prosthetic grafts or vein grafts, when the vein is extensively invaded or occluded by the tumor for more than 50% or when a suture is unfeasible (21). Most authors suggest avoiding SVC reconstruction in the presence of extensive thrombosis invading the subclavian veins due to high risk of thromboembolism or in presence of diffuse collateral venous circulation. If only one brachiocephalic vein is invaded by tumor, it can safely be resected even without replacement (22). Extended operations including resection and reconstruction of the SVC represent a major technical challenge, especially for the potential detrimental effect of clamping a patent vessel, hence it is essential a close cooperation with the anesthesiologist in charge to manage the patient’s hemodynamic as keeping a high cerebral perfusion pressure and administering heparin to prevent potential severe complications. Recently, some authors reported the use of ECC or extra corporeal membrane oxygenation (ECMO) in the surgical management of mediastinal masses (23,24). The assistance of these devices allows an adequate hemodynamic and respiratory function even with lungs deflated and facilitate the dissection of the tumor with a decreased risk of respiratory and hemodynamic decompensation. However, central cannulation may reduce the operative field, hence, peripheral cannulation of the femoral vessels or ECMO should be preferred. However, systemic heparinization required by these devices could increase the risk of hemorrhagic complications during dissection of the tumor as well as the risk of malignant cells spread; therefore, a multidisciplinary risk assessment should be made case-by-case, preoperatively, to assess the need of ECC.
Advanced stage thymoma
Thymomas occurring as large mediastinal masses are often Masaoka-Koga stage III tumors and represent up to 30% of all surgically treated thymomas. In most cases occur involving different intrathoracic structures as pericardium, lung parenchyma, great vessels, phrenic nerve, diaphragm and chest wall. Its treatment is still far from being standardized especially due to its rarity and high variability in clinicopathologic behavior (25). In most series the completeness of resection has been reported as the major prognostic factor associated with prolonged local control and survival, but with a reported rate of radical resection highly variable among them (from 50% to 80%) (26,27). As reported by Attaran and colleagues, a macroscopic incomplete resection or debulking procedures is associated to an increased recurrence rate and to a poorer prognosis without any advantage compared to biopsy alone (26). In literature several reports of extended surgery and reconstruction for thymic malignancies are reported with excellent results in terms of survival and disease local control. The brachiocephalic veins, SVC, lung, pericardium, right atrium, and diaphragm can be safely resected with or without reconstruction increasing the complete resection rate, in the same way, a resection and reconstruction of the aorta and the main pulmonary artery may be indicated in selected cases to achieve complete resection (1). Recently, a survey conducted by the members of the European Association for Cardio-Thoracic Surgery revealed that neoadjuvant therapy (chemo and/or radiation therapy) is currently proposed in the treatment of thymoma to achieve a volume reduction preoperatively with a complete resection rate, after induction therapy, that reaches the 92% while 5-year overall survival (OS) achieves 80% (27). Beyond the discussion on the effectiveness of the induction therapy, an extended total thymectomy, including the tumor together with resection of any invaded adjacent structure, should be considered the main goal of the surgeons, particularly in the setting of stage III thymomas involving great vessels that occurs from 8.9% to 24.8% in major series (21,25). Nevertheless, the involvement of great vessels (brachiocephalic veins, SVC and, even rarely, the aorta and epiaortic vessels) is associated with worse OS (ranging from 45% to 56% at 5 years) compared to those patients with invasion of other surrounding structures in case of radical resection (27). The cause of this high difference is probably related to higher risk of intraoperative severe complications and systemic recurrences, as well as the limited chance of a redo-resection (21). Regarding the involvement of phrenic nerve by thymomas some authors advocate a nerve sparing surgery followed by radiation therapy as a valid option especially in myasthenic patients in order to avoid respiratory complications (20).
Malignant lymphoma may involve the antero-superior mediastinum as a part of disseminated disease or as a primary lesion. The most common types of primary mediastinal lymphomas are Hodgkin’s disease (usually of the nodular sclerosis type), large cell lymphoma (often associated with sclerosis), pulmonary mucosa-associated lymphoid tissue lymphoma and lymphoblastic lymphoma (frequently seen in conjunction with acute lymphoblastic leukemia) (28). Clinical presentation may be similar among different subtypes, as most of these neoplasms generally appear as large invasive anterior mediastinal masses with possible involvement of the surrounding structures. Intensive combination of different chemotherapeutic agents and radiation therapy is the primary treatment modality for mediastinal lymphomas, and surgery is mostly confined to diagnostic biopsies when less invasive procedures like FNA or core biopsy are inconclusive. Some authors, moreover, advocated an important role of surgery also in resection of residual masses after systemic therapy. As reported by Bacha and colleagues, resection of such masses has particularly three purposes: it sets out the need of further treatments, eliminates any residual of tumor cells and reduce the need of adjuvant radiotherapy when the tumor mass is completely removed (19).
GCTs of the mediastinum are uncommon neoplasms and contributing to almost 5% of all mediastinal tumors. These tumors histologically contain the same components as their gonadal counterparts since they are a result of a malignant transformation of arrested germ cells along the urogenital ridge during embryogenesis, but may present different biologic behaviors, clinical characteristics, and poor overall prognoses. They can be divided into three histologic categories: mature teratoma, seminomatous GCT, and non-seminomatous GCT (29). Mature teratomas account for about 60% of all mediastinal GCTs and are characterized by mature tissue derived from all three germinal layers as bone, cartilage, fat, and squamous and glandular epithelia and these tissues may be easily detectable on the CT scan. This kind of tumors are not associated with high level of serum markers like α-FP and β-HCG. Teratoma behavior is extremely variable: the majority present an indolent behavior with adhesion to surrounding structures as main risk, but some mature teratomas can grow more rapidly and may degenerate into non-germ-cell tumors, such as sarcoma and epithelial cancer (30). Surgery is the primary treatment with excellent oncological outcome after complete resection since mature teratomas are not responsive to chemotherapy or radiation therapy. Surgical removal is sometimes challenging especially in case of masses larger than 5 cm or involving the neighboring organs. It has been estimated that approximately 15% of patients requires a resection extended to other structures (e.g., lobectomy, pericardiectomy) for complete tumor resection.
The primary mediastinal seminoma is a rare tumor and typically occurs in men from the second to the fourth decade of life. Typically, these lesions present as a lobulated but homogeneous mass and tend to infiltrate into adjacent structures early in the growth process. Serum tumor markers are usually normal even if high levels of β-HCG can be found in about 40% of patients. Generally, more than one third of patients with mediastinal seminoma have localized disease at the time of diagnosis, while remaining patients have at least one site of distant metastases. Pure seminoma is sensitive to chemotherapy and radiotherapy, and the prognosis is generally good (31). No conclusive data regarding a potential benefit of primary surgery are available and this approach is usually not feasible at presentation, mainly because the disease is rarely diagnosed as a small mediastinal mass with non-extramediastinal invasion. Pure mediastinal seminomas are curable in most patients, even when metastatic at the time of diagnosis. The treatment of choice is a combination of chemo and radiation therapy (32). It has been shown that a residual mass after chemotherapy frequently does not contain viable tumor cells, hence surgery is recommended only for residual masses larger than 3 cm with a growing tendency during surveillance.
Non-seminomatous GCTs are more common than seminoma and include three histologic subtypes, alone or in combination: yolk sac tumor, embryonal carcinoma, and choriocarcinoma (30). These neoplasms present an aggressive behavior causing, in a short time, symptoms by compressing or invading local mediastinal structures and in more than 85% at least one metastatic lesion present at the time of diagnosis. Infiltration into adjacent structures including the lung; the SVC; innominate veins; the pericardium; and, occasionally, other great vessels and the heart can be visible on CT scan. Serum tumor markers (α-FP and β-HCG) are usually abnormal and their high-level in association with typical features on CT scan, is diagnostic of primary malignant non-seminomatous GCTs even without biopsy (32). Approximately 5–10% of patients affected by mediastinal non-seminomatous GCT is associated to Klinefelter syndrome, more rarely these patients present a variety of hematologic neoplasms. Prognosis is poorer when compared with the other GCTs with an average 5-year OS of almost 50%. The role of surgery is very limited because curative results with other treatment modalities are superior moreover in these tumors is extremely important a multi-modal strategy. Most patients have residual radiographic abnormalities in the mediastinum after completion of chemotherapy. In these patients, a radical surgical resection of residual masses should be performed if technically feasible and may be curative in one third of patients (33).
Metastasis in mediastinal lymph nodes are frequently observed in advanced stage lung cancer, thyroid cancer and more seldom in esophageal, pancreatic, colorectal and breast cancer. Stage III non-small cell lung cancer (NSCLC) describes the metastatic spread of a primary tumor to the ipsilateral and/or contralateral mediastinal lymph nodes and include a wide variety of disease ranging from a single station unsuspected N2 disease to large, bulky and invasive N2 or N3 disease that cannot be dissected (34). Bulky nodal disease is generally defined as involvement of lymph nodes with greater than 2 cm short-axis diameter as measured by chest CT, and generally implies extra nodal involvement, multi-station nodal disease, and/or groupings of multiple positive smaller lymph nodes (35). For unresectable N2 or N3 NSCLC concurrent chemoradiotherapy is widely accepted as the standard of care while the role of surgery has been described in very few reports as part of multimodal treatment, but its effectiveness is still far from being recognized (36,37). Thyroid carcinoma consists essentially of 3 histological types: papillary, follicular and medullary carcinomas. The patterns of metastasis of these 3 carcinomas are different. Follicular carcinoma metastasizes predominantly to distant organs such as lung and bone, whereas papillary and medullary carcinomas shows a high incidence of lymph node metastasis, ranging from 30% to 80% of patients, even though metastases to lymph nodes of the upper mediastinum have been found in 9% of patients with thyroid carcinoma. Thyroid cancer commonly develops regional lymphatic metastases into three regions: central, lateral, and mediastinal compartments. There are lots of researches focused on the central and lateral lymph node metastases so far. However, the indications and extent of the mediastinal lymph node dissection in thyroid carcinoma are not clearly defined (38). In these cases, an accurate multidisciplinary assessment is essential and, in case of failure of systemic therapy, most authors advocate that metastatic mediastinal lymph node dissection is an effective treatment in thyroid carcinoma regardless for initial treatment or reoperation of recurrent lesions (39). Nevertheless, medullary thyroid carcinoma cells are not sensitive to radioactive iodine and to hormonal therapy, and, therefore, surgery is the most effective option either with curative intent or effective palliation. Moreover, in case of metastases, redo-surgery should be considered for patients with elevated calcitonin levels in the setting of an incomplete initial surgery, or if there a radiological evidence of recurrent disease. Iterative surgery should be performed in order to reduce the risk of severe compression or invasion of the airways or major vessels. In experienced hands, reoperation for locoregional disease can achieve long-term control and improve the OS in up to one-third of patients (40).
Extended surgery of antero-superior mediastinal masses is a real challenge for the surgeons and the anesthesiologists and should be thoroughly planned step-by-step since the diagnosis. The main goal is obtaining a complete resection of the tumor, that remains the major prognostic factor and allows satisfactory long-term survival. Evolution of the surgical technique end of the peri-operative management as well as the availability of new-generation prosthesis and the increasingly widespread of ECC and ECMO have turned this kind of surgery into a feasible, safe and effective procedure. Centralization of care for patients with these malignancies allows to improve the quality of care that means better surgical and oncological outcome. The preoperative assessment and intraoperative management of these tumors is challenging and a dedicated multidisciplinary approach is essential.
Conflicts of Interest: The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
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Cite this article as: Aprile V, Korasidis S, Bacchin D, Ambrogi MC, Lucchi M. Extended surgery of antero-superior mediastinum. Curr Chall Thorac Surg 2019;1:21.