Spinal Giant Cell Tumor in Neurospine Surgery: A Narrative Study

S. M. Mousavi, N. Kalani, A. Kazeminezhad
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Abstract

Background and Aim: Spinal Giant Cell Tumor (GCT) is a primary low-grade malignant aggressive tumor of the spine and is more prevalent in the third and fourth decades of life. Spinal GCT frequently occurs in the sacrum. The most common presentation of spinal GCT is pain. Spinal GCT is seldom observed as an asymptomatic, incidental radiological occurrence. Based on the clinic-radiological findings, differential diagnoses of spinal GCT are Aneurismal Bone Cyst (ABC), plasmacytoma, symptomatic hemangioma, and Tuberculosis (TB). A biopsy is crucial for a definitive diagnosis. Because of the rich vascular supply about 24 hours prior to operation, Digital Subtraction Angiography (DSA) with tumor embolization is recommended. The treatment of choice for these tumors is complete, extralesional surgical resection which is not usually possible. General treatment is resorted as incomplete partial resection following local radiotherapy. The method of choice for reconstruction is cement or metallic cages and because of the high recurrence rate, bone graft is avoided. The local recurrence rate in the spinal column is lower than in other areas. Methods and Materials/Patients: The spinal GCT incidence, manifestations, diagnosis, and management were concisely reviewed. Using the keywords of GCT, GCT manifestations, GCT complications, GCT management, and GCT incidence, all the relevant articles were retrieved from Google Scholar, Medline, and PubMed, reviewed critically, and analyzed. Results: Spinal GCT rarely presents as an incidental finding in radiologic studies. Because of the high vascular supply of GCTs, preoperative embolization must be performed. The ideal treatment of spinal GCT is complete surgical tumor excision and when not possible, intralesional resection is an alternative treatment. The prognosis of spinal GCT is not good as other primary spinal tumors because of incomplete excision of the tumor and following high recurrence rate. Conclusion: Spinal GCTs are complex clinical entities. Operation is obligatory, and postoperative close follow-up is mandatory to stop recurrences early
脊髓巨细胞瘤在神经脊柱外科:一项叙述性研究
背景和目的:脊柱巨细胞瘤(GCT)是一种原发性低度恶性侵袭性脊柱肿瘤,多见于30岁和40岁。脊髓GCT多发生于骶骨。脊柱GCT最常见的表现是疼痛。脊髓GCT很少被观察到为无症状的偶然放射事件。根据临床影像学表现,脊柱GCT的鉴别诊断为动脉瘤性骨囊肿(ABC)、浆细胞瘤、症状性血管瘤和结核病(TB)。活组织检查对明确诊断至关重要。由于术前24小时左右血管供应丰富,建议采用数字减影血管造影(DSA)联合肿瘤栓塞。对于这些肿瘤的治疗选择是完全的,通常不可能的外伤性手术切除。一般治疗是局部放疗后不完全部分切除。重建的方法选择是水泥或金属笼,由于复发率高,骨移植是避免的。脊柱的局部复发率低于其他部位。方法与材料/患者:对脊柱GCT的发病率、表现、诊断和治疗进行综述。以GCT、GCT表现、GCT并发症、GCT管理、GCT发生率为关键词,从Google Scholar、Medline、PubMed中检索所有相关文献,进行批判性审查和分析。结果:脊柱GCT在放射学研究中很少作为偶然发现。由于gct的高血管供应,术前必须进行栓塞。脊柱GCT的理想治疗方法是完全手术切除肿瘤,当不可能时,病灶内切除是一种替代治疗方法。脊髓GCT由于肿瘤切除不完全,复发率高,预后不如其他原发性脊柱肿瘤好。结论:脊柱gct是复杂的临床实体。手术是必须的,术后密切随访是必须的,以尽早阻止复发
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