基础医学与临床 ›› 2021, Vol. 41 ›› Issue (7): 1066-1070.

• 短篇综述 • 上一篇    下一篇

囊性嗜铬细胞瘤的诊断和治疗进展

杨庭楷1,文进2,纪志刚3,董德鑫4,叶子兴2   

  1. 1. 北京协和医院
    2. 中国医学科学院北京协和医院
    3. 中国医学科学院 北京协和医学院 北京协和医院
    4. 中国医学科学院 北京协和医院泌尿外科
  • 收稿日期:2020-09-29 修回日期:2021-04-26 出版日期:2021-07-05 发布日期:2021-06-17
  • 通讯作者: 文进 E-mail:wjpumch@163.com
  • 基金资助:
    外国文教专家项目管理基金;中国医学科学院中央级公益性科研院所基本科研业务费临床与转化医学研究基金

Progress in diagnosis and treatment of cystic pheochromocytoma

  • Received:2020-09-29 Revised:2021-04-26 Online:2021-07-05 Published:2021-06-17

摘要: 囊性嗜铬细胞瘤是非常罕见的神经内分泌肿瘤,大多无明显临床症状,术前经常不能被准确诊断。当影像学检查发现肾上腺区囊性占位时均应筛查囊性嗜铬细胞瘤的可能。目前最有效的治疗方式是手术切除,腹腔镜肾上腺切除术已成为首选术式,充分的术前准备和严密的术后监护是确保患者围手术期安全的重要前提。

关键词: 囊性嗜铬细胞瘤, 诊断, 治疗

Abstract: Cystic pheochromocytoma is a very rare neuroendocrine tumor, which mostly has no obvious clinical symptoms, and can not be accurately diagnosed before surgery. When a cystic mass in the adrenal gland is found on imaging examination, the possibility of cystic pheochromocytoma should be screened. At present, the most curative treatment is surgical resection. Laparoscopic adrenalectomy has become the first choice. Adequate preoperative preparation and strict postoperative monitoring are important prerequisites for ensuring the safety of patients during the perioperative period.

Key words: Cystic pheochromocytoma, diagnosis, treatment

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