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J Thorac Cardiovasc Surg 2003;125:434-436
© 2003 The American Association for Thoracic Surgery
Brief Communications |
From Department of Surgery, University of Florida, Melbourne, Fla.
Received for publication May 29, 2002. Accepted for publication July 15, 2002. Address for reprints: Michael A. Greene, MD, FCCP, Health First Heart Institute, 1355 S. Hickory Street, Suite 202, Melbourne, FL 32901 (E-mail: mgreene{at}health-first.org).
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Clinical summary
A 48-year-old nonsmoking woman had an approximately 2-year history of intermittent chest discomfort attributed to costochondritis. After a day of vigorous physical exertion, she had acute shortness of breath and right-sided chest pain. She was treated with anti-inflammatory medications. However, a chest radiograph showed a prominent right hilum. She underwent chest computed tomographic and magnetic resonance imaging scans, which demonstrated a large (8.5 cm) anterior mediastinal mass (Figures 1 and 2). A biopsy specimen of the mass was obtained through a small anterior right parasternal incision, and moderately differentiated squamous cell thymic carcinoma was diagnosed (Figure 3).
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The superior vena cava was reconstructed with autologous pericardium. Transient sinus node dysfunction as a result of clamp occlusion of the superior vena caval-right atrial junction was treated during the operation with temporary atrial pacing.
The chest wall soft tissue defect was closed with a pectoralis rotational flap and local fasciocutaneous flap advancement. The patient was extubated after 3 days, with minimal paradoxic right chest wall excursion noted. An elevated right diaphragm as a result of phrenic nerve resection was observed, as expected, on the postoperative chest radiograph.
Oral anticoagulation therapy was started to prevent thrombosis of the extensive pericardial reconstruction of the innominate and superior caval veins. The patient was discharged after 11 days and later returned for outpatient placement of a femoral vein chemotherapy infusion port.
Subsequent treatment included chemotherapy consisting of 6 cycles of paclitaxel at 150 mg/m2 (255 mg) with 6 cycles of carboplatin (540 mg each dose), followed by radiation therapy (Table 1). Preoperative induction radiation of the tumor was considered. However, concerns that the radiation would limit the surgeon's ability to determine tumor margins weighed on the decision to resect first and then apply postoperative radiation.
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Thymic carcinomas comprise only 0.06% of thymic neoplasms. The rarity of these tumors and differences in classification systems combine to make analysis of treatment outcomes problematic. Various treatment combinations with chemotherapy, radiation therapy, and surgery have been used to treat advanced lesions.
3 Radical resections combined with chemotherapy and radiation, such as this case report, have been reported with favorable disease-free survival.
4 Other authors have also noted favorable trends among patients treated with postoperative radiation.
5 Further clinical experience with aggressive multimodality therapy will be necessary to establish optimal protocols for the treatment of these tumors.
References
This article has been cited by other articles:
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C.-C. Chang, Y.-L. Chang, and Y.-C. Lee Thymic carcinoma associated with Sjogren's syndrome and syndrome of inappropriate antidiuretic hormone J. Thorac. Cardiovasc. Surg., February 1, 2010; 139(2): e1 - e2. [Full Text] [PDF] |
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T. De Giacomo, G. Mazzesi, F. Venuta, and G.F. Coloni Extended operation for recurrent thymic carcinoma presenting with intracaval growth and intracardiac extension. J. Thorac. Cardiovasc. Surg., November 1, 2007; 134(5): 1364 - 1365. [Full Text] [PDF] |
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