Xu Shenghan, Yu Ying, Zhang Yajuan, Wen Yong, Li Wei, Huang Tao, Che Bangwei, Zhang Wenjun, Zhang Jinjuan, Tang Kaifa
Department of Urology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Department of Pathology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Front Surg. 2022 Jul 26;9:931998. doi: 10.3389/fsurg.2022.931998. eCollection 2022.
This study shares our experience in managing adrenal schwannoma (AS).
The clinical data of eight patients with AS in our hospital from April 2007 to April 2022 were analyzed retrospectively.
A total of 1309 patients with adrenal lesions were treated in the affiliated hospital of Guizhou Medical University for 15 years, of which only 8 cases were diagnosed as AS, accounting for 0.61%. Among the eight patients with AS, there were five females and three males, with an average age of 48.63 ± 12.05 years, and the average maximum diameter of the tumor was 6.96 ± 1.83 cm. All patients underwent adrenalectomy and were pathologically diagnosed as AS after the operation. The average follow-up time of eight patients with AS was 60.13 ± 22.33 months, and there was no recurrence or metastasis.
The retroperitoneum is an uncommon site for schwannoma tumors, and among adrenal incidentalomas, the schwannoma is rare. The disease lacks specific clinical and imaging features, but correct diagnosis before the pathological examination is very important for clinical management and surgical decision. When imaging examination indicates a slow-growing retroperitoneal mass, schwannoma should be considered. Surgical resection is the main treatment. Pathology is the gold standard for diagnosis. Most of the tumors are benign and have a good prognosis. There is a risk of recurrence after the operation, and it should be monitored actively.
本研究分享我们在肾上腺神经鞘瘤(AS)管理方面的经验。
回顾性分析2007年4月至2022年4月我院8例AS患者的临床资料。
贵州医科大学附属医院15年间共收治1309例肾上腺病变患者,其中仅8例诊断为AS,占0.61%。8例AS患者中,女性5例,男性3例,平均年龄48.63±12.05岁,肿瘤平均最大直径6.96±1.83cm。所有患者均接受了肾上腺切除术,术后病理诊断为AS。8例AS患者平均随访时间为60.13±22.33个月,无复发或转移。
神经鞘瘤在腹膜后是一个不常见的部位,在肾上腺偶发瘤中,神经鞘瘤很少见。该疾病缺乏特异性的临床和影像学特征,但在病理检查前正确诊断对临床管理和手术决策非常重要。当影像学检查提示腹膜后肿块生长缓慢时,应考虑神经鞘瘤。手术切除是主要治疗方法。病理是诊断的金标准。大多数肿瘤为良性,预后良好。术后有复发风险,应积极监测。