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Primary amyloidoma of the spine. A case report and review of the literature.

机译:脊柱原发性淀粉样瘤。病例报告和文献复习。

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STUDY DESIGN: A rare case is reported of primary or idiopathic amyloidoma of the spine derived from production of light chain immunoglobulins. The tumor was successfully treated by anterior decompression and fusion with a fibula strut allograft. OBJECTIVE: To describe a rare case of AL amyloidoma of the spine. SUMMARY OF BACKGROUND DATA: Radiographic characteristics of this benign deposit are similar to harmful aggressive conditions afflicting the spine. RESULTS: The patient returned to full function after the surgery with no evidence of systemic amyloidosis or development of multiple myeloma. METHODS: An isolated AL amyloidoma of the spine was resected and successfully reconstructed with a fibula strut allograft and internal fixation. CONCLUSIONS: Isolated deposits of amyloid in the spine occur very rarely. When no evidence of myeloproliferative disease or systemic amyloidosis is found, prognosis is excellent. The deposit, when it occurs in the spine has a predilection for the thoracic region and can cause neurologic compromise, pain, and deformity that is responsive to decompression and fusion. The diagnosis of primary amyloidoma requires histologic studies for confirmation.
机译:研究设计:罕见病例报道了源自轻链免疫球蛋白产生的原发性或特发性脊柱淀粉样瘤。通过前路减压并与腓骨同种异体植骨融合成功地治疗了该肿瘤。目的:描述一种罕见的脊柱AL淀粉样瘤病例。背景数据总结:这种良性沉积物的放射线照相特征类似于折磨脊柱的有害侵略性疾病。结果:患者在手术后恢复了全部功能,没有系统性淀粉样变性病或多发性骨髓瘤发展的迹象。方法:分离出一个孤立的脊柱AL淀粉样瘤,并用腓骨支杆同种异体移植和内固定术成功重建。结论:很少有淀粉样蛋白沉积在脊柱中。如果没有发现骨髓增生性疾病或系统性淀粉样变性的证据,则预后良好。当沉积物出现在脊柱中时,它倾向于胸腔区域,并可能导致神经系统受损,疼痛和对减压和融合反应敏感的畸形。原发性淀粉样瘤的诊断需要组织学研究以确认。

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