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目的:探讨肾上腺神经鞘瘤的发病特点、诊治方法及预后。方法:回顾性分析5例肾上腺神经鞘瘤患者临床资料。结果:5例术前诊断为无功能性肿瘤2例、嗜铬细胞瘤2例、恶性肿瘤1例,均实施开放手术肿瘤切除术,术后组织病理学检查确诊为肾上腺神经鞘瘤;随访6个月~8 a,未见复发或恶变。结论:肾上腺神经鞘瘤为罕见肾上腺肿瘤,预后良好。其诊断根据组织病理学检查,手术切除为主要治疗方法,术后应定期随访。
Objective: To investigate the incidence of adrenal schwannoma characteristics, diagnosis and treatment methods and prognosis. Methods: The clinical data of 5 patients with adrenal schwannoma were retrospectively analyzed. Results: 5 cases were diagnosed as preoperative non-functional tumor in 2 cases, pheochromocytoma in 2 cases, malignant tumor in 1 case, were performed open surgery tumor resection, postoperative histopathological examination diagnosed as adrenal schwannoma; follow-up 6 Month ~ 8 a, no recurrence or malignant transformation. Conclusion: Adrenal schwannoma is a rare adrenal tumor with a good prognosis. The diagnosis based on histopathological examination, surgical resection as the main method of treatment, should be followed up regularly.