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Abstract Retrosternal goiter was first described by Albrecht von Haller in 1749, as the extension of the thyroid tissue below the upper opening of the chest. The definition of Retrosternal goiter is still not uniform, and varies between the different Authors. However, the most commonly accepted definition of Retrosternal goiter describes a goiter as retrosternal when a ≥ 50% portion of the mass is located in the mediastinum. (Netterville et al., 1998). Diagnosis of Retrosternal goiter is most frequently made in the fifth or sixth decade of life, with a female/male rate of 4:1. retrosternal goiters can be classified as either primary or secondary. Primary intra-thoracic goiters arise from aberrant thyroid tissue which is ectopically located in the mediastinum, receive their blood supply from mediastinal vessels and are not connected to the cervical thyroid. They are rare, representing less than 1% of all retrosternal goiters. (Wu et al., 2006). Secondary retrosternal goiters develop from the thyroid located in its normal cervical site. Downward migration of the thyroid into the mediastinum is facilitated by negative intrathoracic pressure, gravity, traction forces during swallowing and the presence of anatomical barriers preventing the Summary 76 enlargement in other directions (thyroid cartilage, vertebral bodies, strap muscles, especially in patients with a short neck). These secondary retrosternal goiters are, characteristically, in continuity with the cervical portion of the gland and receive their blood supply, depending on cervical vessels, almost always through branches of the inferior thyroid artery. (Shen et al., 2004). The most common symptoms are related to compression of the airways and the esophagus, and are represented by dyspnoea, choking, inability to sleep comfortably, dysphagia and hoarseness. Less commonly, signs of compression of vascular and nervous structures are present, such as superior vena cava obstruction (superior vena cava syndrome) and/or Horner’s syndrome (compression of sympathetic chain). The diagnosis of retrosternal goiter is based upon clinical history, clinical examinations, and imaging findings. (Mackle et al., 2007). Computed tomography (CT) scanning is, at present the most exhaustive examination for assessment of the extent of the goiter and compression effects on adjacent anatomical structures. (Grainger et al., 2005). Most retrosternal goiters can be removed through a cervical approach, while a partial or total sternotomy should be Summary 77 performed only in a minority of patients, ranging between 1- 11%.(Hedayati and McHenry, 2002). There is an alternative and less invasive technique combining video-assisted thoracoscopic surgery (VATS) with a supraclavicular approach. This technique seems to offer improved exposure and reliable control of the neuro-vascular structures in the anterior mediastinum when resecting a huge retrosternal goiter that may prevent nerve injury. (Shigemura et al., 2005). The desire to find a minimally invasive approach to posterior mediastinal tumors stems from increasing evidence that thoracoscopic surgery is associated with quicker recovery and less morbidity than open surgery. (Whitson et al., 2007). The Da Vinci robotic technology offers a novel minimally invasive approach to retrosternal goiters extending into the posterior mediastinum. It appears to be safe and, like VATS, may offer an advantage over an open thoracic approach. Further studies will be required to define its precise role in thyroid surgery. (Augustin et al., 2006). |