Tumors of the Mediastinum and Chest Wall

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Mediastinal Anatomy

The mediastinum is bounded superiorly by the thoracic inlet and inferiorly by the diaphragm. For clinical purposes, the mediastinum has traditionally been divided into the anterior (or anterosuperior), middle, and posterior compartments (Fig. 1). There are no fascial planes between these divisions and they are in continuity with each other. Thus tumors can exist in more than 1 compartment. Nonetheless, these divisions are helpful in forming a differential diagnosis for a mediastinal mass (

Anterior mediastinum

The anterior mediastinum is the most common site of primary mediastinal tumors. Anterior mediastinal masses are malignant in 59% of cases, compared with 29% for middle and 16% for posterior masses.2 The most common primary masses in the anterior mediastinum are lymphomas, thymic neoplasms, germ cell tumors (GCTs), thyroid tissue, parathyroid adenomas, and cysts. Their presentations may range from an incidental finding on a radiograph to debilitating superior vena cava syndrome. Symptomatic

Middle mediastinum

Lymphoma, granulomatous disease, mediastinal cysts, and tracheal tumors are the most common masses in the middle mediastinal. Aside from lymphoma, true tumors of the middle mediastinum are rare. Airway compression and dysphagia are the most common presenting symptoms.

Posterior mediastinum

In the posterior mediastinum, neurogenic tumors and esophageal tumors are the most common masses.2 Neuroenteric cysts are rare foregut malformations that contain both enteric and nerve tissue that are also found in the posterior mediastinum.59 Neurogenic tumors constitute 75% of primary tumors in the posterior mediastinum.2, 60 Most arise from the spinal nerve roots or sympathetic chain and are located in the paravertebral sulcus. Most tumors in the posterior mediastinum are asymptomatic, but

Chest wall tumors

Tumors of the chest wall can be either primary or secondary. The secondary tumors are caused by either local invasion (from breast, lung, or pleural cancers) or distant metastases. Primary chest wall tumors are rare, but include a wide variety of benign and malignant histologies (Table 3). Among primary tumors of the chest wall, roughly half are benign and half are malignant.72

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References (114)

  • Y.J. Cheng et al.

    Videothoracoscopic resection of stage II thymoma: prospective comparison of the results between thoracoscopy and open methods

    Chest

    (2005)
  • E. Davenport et al.

    The role of surgery in the management of thymoma: a systematic review

    Ann Thorac Surg

    (2008)
  • J. Huang et al.

    Feasibility of multimodality therapy including extended resections in stage IVA thymoma

    J Thorac Cardiovasc Surg

    (2007)
  • C.R. Nichols

    Mediastinal germ cell tumors. Clinical features and biologic correlates

    Chest

    (1991)
  • K. Arai et al.

    Primary immature mediastinal teratoma in adulthood

    Eur J Surg Oncol

    (1997)
  • B.D. Lewis et al.

    Benign teratomas of the mediastinum

    J Thorac Cardiovasc Surg

    (1983)
  • P. Macchiarini et al.

    Uncommon primary mediastinal tumours

    Lancet Oncol

    (2004)
  • G.L. Walsh et al.

    Intensive chemotherapy and radical resections for primary nonseminomatous mediastinal germ cell tumors

    Ann Thorac Surg

    (2000)
  • S. Takeda et al.

    Clinical spectrum of mediastinal cysts

    Chest

    (2003)
  • D.C. Strollo et al.

    Primary mediastinal tumors: part II. Tumors of the middle and posterior mediastinum

    Chest

    (1997)
  • U. Cioffi et al.

    Presentation and surgical management of bronchogenic and esophageal duplication cysts in adults

    Chest

    (1998)
  • Y. Kim et al.

    Middle mediastinal lesions: imaging findings and pathologic correlation

    Eur J Radiol

    (2000)
  • T.A. Ishola et al.

    Neuroblastoma

    Surg Oncol

    (2007)
  • G.M. Graeber et al.

    Initial and long-term results in the management of primary chest wall neoplasms

    Ann Thorac Surg

    (1982)
  • G.L. Walsh et al.

    A single-institutional, multidisciplinary approach to primary sarcomas involving the chest wall requiring full-thickness resections

    J Thorac Cardiovasc Surg

    (2001)
  • A.E. Abbas et al.

    Chest-wall desmoid tumors: results of surgical intervention

    Ann Thorac Surg

    (2004)
  • S. Tsukushi et al.

    Soft tissue sarcomas of the chest wall

    J Thorac Oncol

    (2009)
  • P.K. Hsu et al.

    Management of primary chest wall tumors: 14 years' clinical experience

    J Chin Med Assoc

    (2006)
  • M.S. Gordon et al.

    Soft tissue sarcomas of the chest wall. Results of surgical resection

    J Thorac Cardiovasc Surg

    (1991)
  • J.L. Gross et al.

    Soft-tissue sarcomas of the chest wall: prognostic factors

    Chest

    (2005)
  • E.K. Hughes et al.

    Benign primary tumours of the ribs

    Clin Radiol

    (2006)
  • B. O'Connor et al.

    The management of chest wall resection in a patient with polyostotic fibrous dysplasia and respiratory failure

    J Cardiothorac Vasc Anesth

    (2009)
  • S. Kim et al.

    Pediatric rib lesions: a 13-year experience

    J Pediatr Surg

    (2008)
  • S. Basaria et al.

    Images in clinical medicine. Pemberton's sign

    N Engl J Med

    (2004)
  • M.Y. Jeung et al.

    Imaging of cystic masses of the mediastinum

    Radiographics

    (2002)
  • E. Kebebew et al.

    Localization and reoperation results for persistent and recurrent parathyroid carcinoma

    Arch Surg

    (2001)
  • S. Bagga et al.

    Imaging of an invasive malignant thymoma on PET scan: CT and histopathologic correlation

    Clin Nucl Med

    (2006)
  • M.W. Assaad et al.

    Diagnostic accuracy of image-guided percutaneous fine needle aspiration biopsy of the mediastinum

    Diagn Cytopathol

    (2007)
  • V. Annessi et al.

    Ultrasonically guided biopsy of anterior mediastinal masses

    Interact Cardiovasc Thorac Surg

    (2003)
  • K.B. Wilkins et al.

    Clinical and pathologic predictors of survival in patients with thymoma

    Ann Surg

    (1999)
  • D.B. Drachman

    Myasthenia gravis

    N Engl J Med

    (1994)
  • G.B. Blossom et al.

    Thymectomy for myasthenia gravis

    Arch Surg

    (1993)
  • J.M. Buckingham et al.

    The value of thymectomy in myasthenia gravis: a computer-assisted matched study

    Ann Surg

    (1976)
  • A. Masaoka et al.

    Follow-up study of thymomas with special reference to their clinical stages

    Cancer

    (1981)
  • P.M. Schneider et al.

    Prognostic importance of histomorphologic subclassification for epithelial thymic tumors

    Ann Surg Oncol

    (1997)
  • W.D. Travis

    World Health Organization. International Agency for Research on Cancer. Pathology and genetics of tumours of the lung, pleura, thymus and heart

    (2004)
  • G. Cardillo et al.

    Primary neuroendocrine tumours of the thymus: a clinicopathologic and prognostic study in 19 patients

    Eur J Cardiothorac Surg

    (2010)
  • K. Ogawa et al.

    Postoperative radiotherapy for patients with completely resected thymoma: a multi-institutional, retrospective review of 103 patients

    Cancer

    (2002)
  • O. Rena et al.

    Does adjuvant radiation therapy improve disease-free survival in completely resected Masaoka stage II thymoma?

    Eur J Cardiothorac Surg

    (2007)
  • M. Okumura et al.

    Outcome of surgical treatment for recurrent thymic epithelial tumors with reference to World Health Organization histologic classification system

    J Surg Oncol

    (2007)
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