期刊
ANNALS OF THORACIC SURGERY
卷 101, 期 4, 页码 1594-1596出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.athoracsur.2015.05.130
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Primary neuroendocrine neoplasms of the mediastinum are extremely rare. We report the case of a 54-year-old woman who presented with dyspnea and was found to have a 6.8-cm tumor completely obliterating the right main pulmonary artery. Analysis of an endobronchial ultrasound fine-needle aspiration revealed a neuroendocrine tumor. A positron emission tomography scan showed no evidence of distant disease. The patient underwent surgical resection with reconstruction of the right main pulmonary artery with a Dacron (DuPont, Wilmington, DE) graft, followed by chemoradiotherapy. We discuss the presentation and management of this patient and review the current treatment options of primary neuroendocrine carcinomas of the mediastinum. (C) 2016 by The Society of Thoracic Surgeons
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