Yajima H, Sakaguchi H, Tomoyasu H, Tanimura S, Bamba J, Masaki M
Department of Thoracic Surgery, Toranomon Hospital, Tokyo, Japan.
Nihon Kyobu Geka Gakkai Zasshi. 1997 Feb;45(2):155-60.
The patient was a 20-year-old male. On routine check-ups, a posterior mediastinal tumor was found radiologically and referred to our hospital for the operation. During the Video-Assisted Thoracic Surgery (VATS), sudden elevation of the blood pressure up to 270 mmHg was observed by the tumor palpation. At once we diagnosed as pheochromocytoma. Changing the VATS to usual thoracotomy the tumor was completely removed and histologically confirmed. After the operation the patient was uneventful and the value of norèpinephrine reduced to normal range from 2912 pg/ml. The posterior mediastinal pheochromocytoma is rare and this report is the 6 th case in Japan. Clinical characteristics were discussed in addition to the review of the literature.
该患者为一名20岁男性。在常规体检中,经放射检查发现后纵隔肿瘤,并转诊至我院接受手术。在电视辅助胸腔镜手术(VATS)过程中,触诊肿瘤时观察到血压突然升至270 mmHg。我们立即诊断为嗜铬细胞瘤。将VATS改为常规开胸手术,肿瘤被完全切除并经组织学证实。术后患者情况平稳,去甲肾上腺素值从2912 pg/ml降至正常范围。后纵隔嗜铬细胞瘤较为罕见,本报告是日本的第6例。除了文献回顾外,还讨论了临床特征。