Myasthenia gravis is an autoimmune disease of the neuromuscular junction (NMJ), characterized by weakness and fatigue of skeletal muscles (1). The main cause of this disease is antibodies targeting acetylcholine receptor in the neuromuscular synapse, which leads to impaired signal transduction between the nervous and musculoskeletal system (2).
Myasthenia gravis is a relatively uncommon disease with the estimated prevalence rate between 70 and 163 people per million, which mostly occurs in women in the third and fourth decades of life (3–5).
Myasthenia gravis has the potential to affect any skeletal muscle, but it mostly presents with significant disruptions in the muscles involved in eye movement, swallowing, blinking, and facial expressions (6, 7). Hence, ptosis, changes in facial expression, double vision, swallowing dysfunction, fluctuating fatigable weakness, speech impairments, respiratory issues, and paralysis are expected signs and symptoms in the patients (8, 9).
The most important feature is the history of fluctuating fatigable weakness which leads to the clinical diagnosis of the disease (10).
The ice pack test, the Mestinon test, the Tensilon test and measurement of anti-acetylcholine receptor antibodies (Anti-AChRAbs) and Muscle-specific receptor kinase tyrosine-specific (MuSK) antibodies in the serum are additional tests that can provide considerable assistance in diagnosing this condition (11).Approximately 90% of patients suffered from myasthenia gravis are seropositive for anti-acetylcholine receptor antibodies (Anti-AChRAbs) (12).
Thymoma and thymic carcinoma are the most prevalent tumors of thymus gland which usually occur between fourth and sixth decades of life and account for approximately 20% of mediastinal neoplasms (13, 14).
Anterior mediastinal masses have a higher Risk of being malignant compared to middle and posterior mediastinal masses. Malignant anterior mediastinal masses predominantly including thymoma, lymphoma, germ cell tumors, and tumors of the thyroid and parathyroid glands (15, 16). Different symptoms are associated with the presence of malignant masses, including chest pain, dyspnea, cough, phrenic nerve paralysis, superior vena cava syndrome, and other symptoms such as night sweats, weight loss, and fever. Thymic carcinomas prognosis are worse than thymomas, and necrotic and calcification regions with irregular borders are visible in imaging (14, 17). The most common paraneoplastic syndrome associated with thymoma, is myasthenia gravis which is found in at least 50% of the patients (18).
Thymectomy leads to improvement in approximately 75% of patients with myasthenia gravis, with complete remission in 30% of cases. While thymectomy may have greater benefits in younger patients, optimal outcomes have been reported in both younger and older age groups (19–22). Thymectomy is performed in patients with myasthenia gravis due to thymic abnormalities, with most cases having thymic hyperplasia (85%) or thymoma (15%). The procedure is safe and effective, even in pediatric patients, and studies demonstrate that some factors such as age under 35, Presence of symptoms less than 24 months before the operation and no prior history of steroid treatment to be associated with better outcomes in patients(21, 23, 24).
Generally, thymectomy can be performed in four main methods: trans-cervical thymectomy, video-assisted thoracoscopic surgery (VATS), trans-sternal thymectomy, and a combination of trans-cervical and trans-sternal thymectomy (25). In all these methods, the thymic tissue is resected, but the resection of extra-capsular mediastinal tissue and cervical fat tissue varies. Some surgeons prefer the trans-sternal approach due to extensive approach for thorough exploration of the mediastinum up to the neck and enables complete removal of thymic tissue and fat (25, 26).
On the other hand, one of the best surgical approaches for thymectomy is video-assisted thoracoscopic surgery (VATS), which is considered a less invasive method and suitable for patients with a diagnosis of myasthenia gravis. Some studies have shown that using minimally invasive techniques such as video-assisted and robot-assisted approaches are associated with fewer complications and mortality compared to trans-sternal techniques, while achieving similar therapeutic outcomes(27).
However, considering the inconsistent results of various studies, it seems that more extensive research is still needed to investigate the outcomes of different surgical techniques in patients with myasthenia gravis. Therefore, in the present study, we focused on evaluating patients with myasthenia gravis who underwent thoracoscopic thymectomy and examined the long-term results.