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J Thorac Cardiovasc Surg 2006;132:705-706
© 2006 The American Association for Thoracic Surgery
Brief Communication |
Department of Cardiothoracic Surgery, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Received for publication January 23, 2006; accepted for publication February 22, 2006. * Address for reprints: Jun Matsumoto, MD, Division of Surgery, Asahi General Hospital, I-1326 Asahi, Chiba, Japan (Email: matsumoto{at}hospital.asahi.chiba.jp).
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Middle mediastinal paragangliomas are very rare, slow-growing tumors, but almost all of them are very hypervascular tumors. Complete surgical resection is difficult to achieve because of their proximity to the heart, great vessels, and trachea. We report successful complete resection incorporating preoperative embolization and a clamshell bilateral thoracotomy.
Clinical Summary
A 52-year-old woman was found to have an abnormal shadow on a chest radiograph for a medical checkup. Chest computed tomography at another hospital revealed a large well-enhanced mass with a cystic lesion located between the superior vena cava, aortic arch, right pulmonary artery, left atrium, and trachea (Figures 1 and 2).
A video-assisted thoracoscopic biopsy was performed at another hospital to make the diagnosis, but massive bleeding occurred during the procedure, and the biopsy was abandoned. The patient was then referred to our department. We strongly suspected a paraganglioma of the middle mediastinum. The serum noradrenaline level was slightly increased, and an iodine 123meta-iodobenzylguanidine scan showed uptake in the tumor. An angiographic study showed many feeding arteries, and the main feeders were 3 thick bronchial arteries. Preoperative embolization with Gelfoam (Pfizer, Ann Arbor, Mich) and several microcoils was performed the day before the operation. At operation, we were ready to perform cardiopulmonary bypass; however, complete resection of the tumor without cardiopulmonary bypass was performed via the clamshell approach. Finally, intraoperative blood loss was reduced to 1070 mL. Histologic diagnosis was reported as a typical paraganglioma, 7 cm in size. There was no sign of recurrence on a computed tomography scan 1 year after surgery.
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Aorticopulmonary paragangliomas are rare neoplasms; 79 anterior and middle mediastinal paragangliomas, which represent a surgical challenge, were reviewed.1
Because of their location close to the great vessels and trachea, complete resection is very difficult. Paragangliomas are locally invasive and have a high local recurrence rate (55.7%) and metastatic potential (26.6%). Radiation and chemotherapy seem to be ineffective. Complete resection is an important prognostic factor.1
Preoperative embolization for posterior mediastinal paraganglioma was first described in 19872
and minimizes perioperative vascular complications.3
In our case, preoperative embolization of the three main feeders (bronchial arteries) was performed the day before surgery, and it reduced intraoperative blood loss and permitted dilated bronchial arteries behind the tumor to be ligated and divided more safely.
The surgical approach we selected was the clamshell approach, which was described by Bains and coworkers.4
It provides a better view of lateral and posterior aspects of the tumor than median sternotomy, but it causes longer-lasting pain and more impaired postoperative respiratory function than median sternotomy. In our case, the intraoperative view was excellent, and complete resection was achieved more safely than it would have been by median sternotomy.
In a few of the cases that have been reported, surgery was performed with the help of cardiopulmonary bypass.1,5
Cardiopulmonary bypass should be available and used if necessary for complete resection in cases in which there is local invasion to vital structures.
Almost all aorticopulmonary paragangliomas are aggressive and locally invade vital structures. A careful perioperative strategy (eg, preoperative embolization, an appropriate surgical approach, and cardiopulmonary bypass) is required to resect them completely.
References
This article has been cited by other articles:
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P.-Y. Brichon, O. Chavanon, P. Chaffanjon, F. Thony, N. Wion-Barbot, and G. Ferretti A Mediastinal Paraganglioma Mimicking a Large Tracheobronchial Invasion Ann. Thorac. Surg., August 1, 2010; 90(2): e30 - e30. [Full Text] [PDF] |
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M.-W. Lin, Y.-L. Chang, Y.-C. Lee, and P.-M. Huang Non-functional paraganglioma of the posterior mediastinum Interact CardioVasc Thorac Surg, September 1, 2009; 9(3): 540 - 542. [Abstract] [Full Text] [PDF] |
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M. L. Brown, G. E. Zayas, M. D. Abel, W. F. Young Jr, and H. V. Schaff Mediastinal Paragangliomas: The Mayo Clinic Experience Ann. Thorac. Surg., September 1, 2008; 86(3): 946 - 951. [Abstract] [Full Text] [PDF] |
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