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Clinical features and prognosis analysis of metastatic spinal pheochromocytoma: A single center retrospective study

机译:转移性脊髓细胞瘤细胞瘤的临床特征及预后分析:单一中心回顾性研究

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Purpose Metastatic spinal pheochromocytoma (MSP) is very rare in clinical practice, with only a few case reports in the literature. Its low incidence makes it profoundly difficult for clinicians to determine appropriate treatment strategies and predict the prognosis. In this study, we analyzed the clinical characteristics, surgical procedure and prognosis of patients with MSP in one of the largest clinical investigations of this entity to date. Methods In this study, we conducted a retrospective analysis of the clinical data of 10 patients with MSP who were treated in our department from 2012 to 2020. We performed a total of 14 operations using two types of surgery: open surgery and percutaneous vertebroplasty. Results Among them, nine patients underwent 14 spinal operations with satisfactory effect and without any perioperative complications. The mean time from the initial operation to detection of spinal metastasis was 85.3 (12–132) months. The average follow-up time was 27.3?months. Disease progression was detected in nine patients, and eight patients (80%) died during the follow-up period. Univariate analysis showed that extraosseous visceral metastasis ( P =?0.022), Tomita score ( P =?0.027), and number of spinal metastases ( P =?0.024) were associated with overall survival (OS). In addition, extraosseous visceral metastasis ( P =?0.030), Tomita score ( P =?0.013), and number of spinal metastases ( P =?0.026) were associated with progression-free survival (PFS). Conclusions Surgical treatment is an effective option in treating MSP and plays an important role in improving patients’ quality of life, due to its efficacy in relieving pain, reconstruction of stability, and restoration of function. Extraosseous metastasis, Tomita score, and number of spinal metastases are all potential prognostic factors for OS and PFS.
机译:目的转移性脊髓嗜铬细胞瘤(MSP)在临床实践中非常罕见,在文献中只有几个报告。它的低发病率使临床医生难以确定适当的治疗策略并预测预后。在这项研究中,我们分析了MSP患者迄今为止最大的临床调查之一的临床特征,外科手术和预后。方法在本研究中,我们对2012年至2020年在我们的部门治疗的MSP患者的临床数据进行了回顾性分析。我们使用两种外科进行了14种操作:开放式手术和经皮椎体术。结果,九名患者接受了14名脊柱作用的效果令人满意,没有任何围攻并发症。初始操作的平均时间脊髓转移检测为85.3(12-132)个月。平均随访时间为27.3个月。在九个患者中检测到疾病进展,并在后续期间死亡8名患者(80%)。单变量分析表明,异构内脏转移(P = 0.022),Tomita得分(P = 0.027),脊柱转移数(P = 0.024)与总存活(OS)相关。此外,特征内脏转移(P = 0.030),Tomita得分(P = 0.013),脊柱转移数(P = 0.026)与无进展存活(PFS)相关。结论外科治疗是治疗MSP的有效选择,并在提高患者的生活质量方面发挥重要作用,因为它在缓解疼痛,重建稳定性和恢复功能的疗效中,效果。异形转移,Tomita评分和脊柱转移数是OS和PFS的潜在预后因素。

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